ClinVar Miner

Variants studied for cerebral malformation with epilepsy

Included ClinVar conditions (173):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign risk factor not provided total
954 484 4702 1595 1176 3 15 8616

Gene and significance breakdown #

Total genes and gene combinations: 149
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign risk factor not provided total
RELN 14 9 651 216 66 0 1 904
FLNA 68 31 392 239 123 0 3 844
FKTN 33 25 243 77 24 0 0 380
FKRP 41 12 190 86 11 0 0 337
CDON 4 0 157 37 86 0 0 281
QARS1 22 7 201 51 1 0 0 279
TSC1 5 1 157 32 84 0 0 277
POMT1 31 14 136 51 28 0 0 256
POMT2 24 8 154 52 15 0 2 251
LOC101927870, RELN 0 2 162 56 21 0 0 234
DAG1 8 1 155 44 10 0 0 217
GLI2 13 2 94 63 61 0 0 215
POMGNT2 8 2 136 57 11 0 0 214
COL4A2 5 4 76 23 108 0 0 213
COL4A1 24 14 78 62 90 0 1 212
RAB3GAP2 6 1 131 41 22 0 1 193
PTCH1 3 1 102 38 50 0 0 189
CRPPA 30 8 84 25 13 0 0 159
ARFGEF2 5 2 138 4 9 0 1 158
ADGRG1 21 6 83 13 22 0 0 140
POMGNT1, TSPAN1 10 72 51 12 7 0 0 140
B3GALNT2 16 11 83 29 4 0 0 135
PAFAH1B1 89 31 10 0 2 0 1 128
GMPPB 15 8 67 30 4 0 0 123
SLC9A6 18 5 58 28 14 0 0 121
RAB18 5 0 80 5 29 0 0 119
ACTB 28 18 24 31 16 0 0 113
LARGE1 5 1 77 9 21 0 0 113
RAB3GAP1 26 1 57 8 19 0 0 111
POMK 11 0 59 28 7 0 0 101
FOXH1 0 0 49 16 19 0 0 81
TUBA1A 28 43 12 0 0 0 2 73
MYH11, NDE1 0 0 40 9 23 0 0 72
B4GAT1 2 1 41 21 5 0 0 69
SHH 37 4 14 8 9 0 0 68
ACTG1 8 9 8 17 23 0 0 63
NDE1 7 0 40 5 10 0 0 61
NODAL 0 0 30 6 12 0 0 48
ZIC2 18 6 12 5 7 0 0 48
TSC2 9 3 32 0 0 0 0 44
LAMC3 5 0 20 2 13 0 0 40
TUBB2B 8 12 17 1 1 0 0 37
FLNA, LOC107988032 4 2 22 4 5 0 0 36
TGIF1 7 1 6 12 16 0 0 34
SIX3 12 2 8 3 9 0 0 32
PSAT1 5 0 13 9 4 0 0 31
RXYLT1 8 4 18 2 2 0 0 31
DCX 19 9 2 1 0 0 0 29
ADGRG1, ADGRG3 0 0 16 1 11 0 0 28
ARX 24 2 2 0 0 0 0 28
LOC100507346, PTCH1 2 0 11 9 6 0 0 27
MACF1 6 1 18 2 0 0 0 26
POMGNT1 1 8 11 1 0 0 0 21
RTTN 6 0 14 0 1 0 0 21
TUBB3 7 7 9 0 0 0 0 21
DYNC1H1 0 13 6 0 0 0 0 19
PHGDH 8 3 8 0 0 0 0 17
B3GALNT2, TBCE 1 1 11 3 0 0 0 16
MTOR 9 0 6 0 0 0 1 16
FGF8 1 9 3 1 1 0 0 15
FOXH1, KIFC2 0 0 11 1 3 0 0 15
LAMB1 4 0 10 1 0 0 0 15
NEDD4L 4 3 9 0 0 0 0 15
TUBB2A 3 9 5 0 1 0 0 15
MAP1B 7 4 4 0 0 3 0 11
PI4KA 3 1 7 0 0 0 0 11
TUBB 5 3 3 0 0 0 1 10
COL4A1, COL4A2 0 0 0 2 7 0 0 9
ARX, LOC109610631 6 1 1 0 0 0 0 8
CEP85L 6 1 1 0 0 0 0 8
FIG4 5 1 2 0 0 0 0 8
KIF2A 4 3 2 0 0 0 0 8
TUBA8 0 0 8 0 0 0 0 8
KATNB1 6 0 1 0 0 0 0 7
KIF5C 2 0 3 2 0 0 1 7
TBC1D20 5 0 2 0 0 0 0 7
TMTC3 5 1 2 0 0 0 0 7
TUBG1 3 2 1 1 0 0 0 7
​intergenic 3 0 1 0 2 0 0 6
EML1 5 1 0 0 0 0 0 6
ERMARD 1 0 2 1 1 0 0 5
LMBR1, SHH, ZRS 0 0 0 0 5 0 0 5
APC2 4 0 0 0 0 0 0 4
ARF1 3 1 0 0 0 0 0 4
COLGALT1 4 0 0 0 0 0 0 4
CTNNA2 3 0 1 0 0 0 0 4
EMX2 4 0 0 0 0 0 0 4
FGFR1 1 3 0 0 0 0 0 4
LAMA5 0 0 4 0 0 0 0 4
STAG2 3 0 0 1 0 0 0 4
DISP1 0 0 3 0 0 0 0 3
DNASE1L1, EMD, FLNA, RPL10, TAFAZZIN 0 0 3 0 0 0 0 3
LOC110008580, ZIC2 2 0 1 0 0 0 0 3
MIR484, NDE1 0 0 2 1 0 0 0 3
ATP1A2 2 0 0 0 0 0 0 2
CELSR1 0 0 2 0 0 0 0 2
CNOT1 1 0 2 0 0 0 0 2
DLL1 0 0 2 0 0 0 0 2
EMD, FLNA 0 0 2 0 0 0 0 2
GAS1 0 0 2 0 0 0 0 2
LAMA2 0 0 2 0 0 0 0 2
LINGO4 0 0 2 0 0 0 0 2
PLOD1 2 0 0 0 0 0 0 2
PTEN 2 0 0 0 0 0 0 2
ABAT, ABCA3, ABCC1, ABCC6, ACSM1, ACSM2A, ACSM2B, ACSM3, ACSM5, ADCY9, AHSP, ALDOA, ALG1, AMDHD2, ANKS3, ANKS4B, APOBR, AQP8, ARHGAP17, ARL6IP1, ARMC5, ASPHD1, ATF7IP2, ATP2A1, ATP6V0C, ATXN2L, BAIAP3, BCAR4, BCKDK, BCL7C, BFAR, BICDL2, BMERB1, BOLA2, BOLA2B, BRICD5, C16orf54, C16orf72, C16orf82, C16orf89, C16orf90, C16orf91, C16orf92, C16orf96, CACNG3, CARHSP1, CASKIN1, CCDC154, CCDC189, CCNF, CCP110, CD19, CD2BP2, CDIP1, CDIPT, CDR2, CEMP1, CEP20, CHP2, CIITA, CLCN7, CLDN6, CLDN9, CLEC16A, CLEC19A, CLN3, CLUAP1, COG7, COQ7, CORO1A, CORO7, CORO7-PAM16, COX6A2, CPPED1, CRAMP1, CREBBP, CRYM, CTF1, DCTN5, DCTPP1, DCUN1D3, DEXI, DNAAF8, DNAH3, DNAJA3, DNASE1, DNASE1L2, DOC2A, E4F1, EARS2, ECI1, EEF2K, EEF2KMT, EIF3C, EIF3CL, ELOB, EME2, EMP2, ERCC4, ERI2, ERN2, FAHD1, FBRS, FBXL19, FLYWCH1, FLYWCH2, FUS, GDE1, GDPD3, GFER, GGA2, GLIS2, GLYR1, GNPTG, GP2, GPR139, GPRC5B, GRIN2A, GSG1L, GSPT1, GTF3C1, HAGH, HCFC1R1, HIRIP3, HMOX2, HS3ST2, HS3ST4, HS3ST6, HSD3B7, IFT140, IGFALS, IGSF6, IL21R, IL27, IL32, IL4R, INO80E, IQCK, ITGAD, ITGAL, ITGAM, ITGAX, ITPRIPL2, JPT2, KAT8, KATNIP, KCTD13, KCTD5, KDM8, KIF22, KNOP1, KREMEN2, LAT, LCMT1, LDAF1, LITAF, LYRM1, MAPK3, MAPK8IP3, MARF1, MAZ, MEFV, MEIOB, METTL22, METTL9, MGRN1, MIR1225, MIR193B, MIR365A, MLST8, MMP25, MOSMO, MPV17L, MRPS34, MRTFB, MSRB1, MTRNR2L4, MVP, MYH11, MYLPF, NAA60, NAGPA, NDE1, NDUFAB1, NDUFB10, NFATC2IP, NLRC3, NME3, NMRAL1, NOMO1, NOMO2, NOMO3, NOXO1, NPIPA1, NPIPA2, NPIPA3, NPIPA5, NPIPB3, NPIPB4, NPIPB5, NPIPB6, NPW, NSMCE1, NTAN1, NTHL1, NTN3, NUBP1, NUBP2, NUDT16L1, NUPR1, OR1F1, OR2C1, ORAI3, OTOA, PAGR1, PALB2, PAM16, PAQR4, PARN, PDILT, PDPK1, PDXDC1, PDZD9, PGP, PHKG2, PKD1, PKMYT1, PLA2G10, PLK1, PMM2, POLR3E, PPL, PPP4C, PRKCB, PRM1, PRM2, PRM3, PRR14, PRRT2, PRSS21, PRSS22, PRSS27, PRSS33, PRSS36, PRSS41, PRSS53, PRSS8, PTX4, PYCARD, PYDC1, QPRT, RAB26, RABEP2, RBBP6, RBFOX1, RMI2, RNF151, RNF40, RNPS1, ROGDI, RPL3L, RPS15A, RPS2, RRN3, RSL1D1, RUSF1, SBK1, SCNN1B, SCNN1G, SDR42E2, SEC14L5, SEPHS2, SEPTIN1, SEPTIN12, SETD1A, SEZ6L2, SGF29, SH2B1, SHISA9, SLC5A11, SLC5A2, SLC9A3R2, SLX1A, SLX1B, SLX4, SMG1, SMIM22, SNHG9, SNN, SNX29, SOCS1, SPN, SPNS1, SPSB3, SRCAP, SRL, SRRM2, STX1B, STX4, SULT1A1, SULT1A2, SULT1A3, SULT1A4, SYNGR3, SYT17, TAOK2, TBC1D10B, TBC1D24, TBL3, TBX6, TEDC2, TEKT5, TELO2, TFAP4, TGFB1I1, THOC6, THUMPD1, TIGD7, TLCD3B, TMC5, TMC7, TMEM114, TMEM186, TMEM204, TMEM219, TNFRSF12A, TNFRSF17, TNP2, TNRC6A, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D, TPSAB1, TPSB2, TPSD1, TRAF7, TRAP1, TRIM72, TSC2, TSR3, TUFM, TVP23A, TXNDC11, UBALD1, UBE2I, UBFD1, UBN1, UMOD, UNKL, UQCRC2, USP31, USP7, VASN, VKORC1, VPS35L, VWA3A, XPO6, XYLT1, YPEL3, ZC3H7A, ZG16, ZG16B, ZKSCAN2, ZNF174, ZNF200, ZNF205, ZNF213, ZNF263, ZNF267, ZNF48, ZNF500, ZNF597, ZNF598, ZNF629, ZNF646, ZNF668, ZNF688, ZNF689, ZNF720, ZNF747, ZNF75A, ZNF764, ZNF768, ZNF771, ZNF785, ZNF843, ZP2, ZSCAN10, ZSCAN32 1 0 0 0 0 0 0 1
ABCC4, CLDN10, CLYBL, DCT, DNAJC3, DOCK9, DZIP1, FARP1, FGF14, GGACT, GPC5, GPC6, GPR18, GPR180, GPR183, HS6ST3, IPO5, ITGBL1, MBNL2, METTL21C, MIR17, MIR17HG, MIR18A, MIR19A, MIR19B1, MIR20A, MIR92A1, NALCN, OXGR1, PCCA, RAP2A, RNF113B, SLC15A1, SOX21, STK24, TGDS, TM9SF2, TMTC4, TPP2, UBAC2, UGGT2, ZIC2, ZIC5 1 0 0 0 0 0 0 1
ABL1, AIF1L, EXOSC2, FAM78A, FIBCD1, LAMC3, NUP214, PLPP7, POMT1, PRDM12, PRRC2B, QRFP 0 0 1 0 0 0 0 1
ACP6, BCL9, CHD1L, FMO5, GJA5, GJA8, GPR89B, PRKAB2 1 0 0 0 0 0 0 1
AIPL1 0 0 0 0 1 0 0 1
AKT3 0 1 0 0 0 0 0 1
AMT, C3orf62, C3orf84, CCDC71, DAG1, GPX1, IHO1, KLHDC8B, LAMB2, NICN1, RHOA, TCTA, USP4 1 0 0 0 0 0 0 1
ANKMY2, BZW2, CRPPA, LRRC72, SOSTDC1 1 0 0 0 0 0 0 1
ASPA, CLUH, LOC100288728, METTL16, OR1A1, OR1A2, OR1D2, OR1D5, OR1E1, OR1E2, OR1G1, OR3A1, OR3A2, OR3A3, PAFAH1B1, RAP1GAP2, SPATA22, TRPV3 1 0 0 0 0 0 0 1
BAG6 0 0 1 0 0 0 0 1
BOC 0 0 1 0 0 0 0 1
BORCS5 0 1 0 0 0 0 0 1
CALM3, DACT3, FKRP, GNG8, PRKD2, PTGIR, STRN4 0 0 1 0 0 0 0 1
CDK5 1 0 0 0 0 0 0 1
CENPJ 0 1 0 0 0 0 0 1
CLUH, METTL16, PAFAH1B1, RAP1GAP2 1 0 0 0 0 0 0 1
CLYBL, TM9SF2, UBAC2, ZIC2, ZIC5 1 0 0 0 0 0 0 1
COLGALT1, NIBAN3 0 1 0 0 0 0 0 1
DHX37 0 1 0 0 0 0 0 1
DPH1, HIC1, INPP5K, METTL16, MIR132, MIR212, MIR22, MNT, MYO1C, OVCA2, PAFAH1B1, PITPNA, PRPF8, RILP, RPA1, RTN4RL1, SCARF1, SERPINF1, SERPINF2, SGSM2, SLC43A2, SMG6, SMYD4, SRR, TLCD2, TSR1, WDR81 1 0 0 0 0 0 0 1
EHMT1 1 0 0 0 0 0 0 1
ENTPD1 0 0 1 0 0 0 0 1
EXOSC3 1 0 0 0 0 0 0 1
FHL1, SLC9A6 0 0 1 0 0 0 0 1
FKRP, STRN4 0 0 1 0 0 0 0 1
FKTN, FSD1L 1 0 0 0 0 0 0 1
FNTA, HOOK3, MIR4469, POMK, RNF170, THAP1 0 0 1 0 0 0 0 1
FOXG1 0 1 0 0 0 0 0 1
GRIN1 0 0 1 0 0 0 0 1
LOC102724058, SCN1A 1 0 0 0 0 0 0 1
MATN4 0 1 0 0 0 0 0 1
NBN 1 0 0 0 0 0 0 1
NKX2-5 0 0 0 0 1 0 0 1
NR2F1 0 0 1 0 0 0 0 1
NSDHL 0 0 1 0 0 0 0 1
OFD1 0 1 0 0 0 0 0 1
PEX1 0 0 1 0 0 0 0 1
PIK3CA 0 0 1 0 0 0 0 1
RHEB 0 1 0 0 0 0 0 1
RPS6 0 0 1 0 0 0 0 1
SCN3A 0 1 0 0 0 0 0 1
SETD5 0 1 0 0 0 0 0 1
TUBA3E 0 1 0 0 0 0 0 1
WDR81 1 0 0 0 0 0 0 1
ZRSR2 0 1 0 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 130
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign risk factor not provided total
Invitae 247 85 2756 1205 467 0 0 4760
Illumina Clinical Services Laboratory,Illumina 2 1 1476 366 726 0 0 2516
OMIM 383 0 5 0 0 0 0 388
Genetic Services Laboratory, University of Chicago 144 49 38 0 0 0 0 231
Baylor Genetics 42 20 139 1 0 0 0 202
Fulgent Genetics,Fulgent Genetics 16 5 142 0 0 0 0 163
Counsyl 5 70 32 3 0 0 0 110
GeneReviews 85 0 0 0 16 0 0 101
Natera, Inc. 8 1 51 14 13 0 0 87
Centre for Mendelian Genomics,University Medical Centre Ljubljana 12 8 53 3 4 0 0 80
University of Washington Center for Mendelian Genomics, University of Washington 0 46 12 0 0 0 0 58
Institute of Human Genetics, University of Leipzig Medical Center 6 14 20 3 0 0 0 43
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 1 7 30 0 0 38
Mendelics 5 8 6 5 13 0 0 37
Juha Muilu Group; Institute for Molecular Medicine Finland (FIMM) 1 36 0 0 0 0 0 37
Claritas Genomics 8 15 6 0 0 0 0 29
Muenke lab,National Institutes of Health 12 7 9 0 1 0 0 29
Athena Diagnostics Inc 0 0 0 0 28 0 0 28
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 6 3 19 0 0 0 0 28
Genomic Research Center, Shahid Beheshti University of Medical Sciences 4 4 18 0 0 0 0 26
Biochemical Molecular Genetic Laboratory,King Abdulaziz Medical City 7 8 6 0 0 0 0 21
Institute of Human Genetics, Klinikum rechts der Isar 11 8 0 0 0 0 0 19
Service de Génétique Moléculaire,Hôpital Robert Debré 5 5 4 5 0 0 0 19
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine 0 6 13 0 0 0 0 19
Broad Institute Rare Disease Group, Broad Institute 3 3 6 0 4 0 0 16
Department of Genetics,Robert DEBRE University Hospital 15 0 0 0 0 0 0 15
GenomeConnect, ClinGen 0 0 0 0 0 0 14 14
New York Genome Center 1 0 12 0 0 0 0 13
Génétique des Maladies du Développement, Hospices Civils de Lyon 5 4 3 0 0 0 0 12
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories 1 0 1 1 8 0 0 11
Laboratory of Molecular Genetics,CHU RENNES 0 7 4 0 0 0 0 11
Bruce Lefroy Centre, Murdoch Childrens Research Institute 1 7 1 0 0 0 0 9
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 4 1 3 0 0 0 0 8
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 3 5 0 0 0 0 0 8
Genomic Medicine Lab, University of California San Francisco 4 2 2 0 0 0 0 8
Genetics Institute, Tel Aviv Sourasky Medical Center 3 5 0 0 0 0 0 8
Integrated Genetics/Laboratory Corporation of America 5 2 0 0 0 0 0 7
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 2 3 2 0 0 0 0 7
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine 2 4 0 0 0 0 0 6
Hehr Laboratory,Center for Human Genetics - University of Regensburg 0 4 2 0 0 0 0 6
Mayo Clinic Laboratories, Mayo Clinic 1 2 3 0 0 0 0 6
NeuroMeGen,Hospital Clinico Santiago de Compostela 0 5 1 0 0 0 0 6
Molecular Genetics Laboratory,BC Children's and BC Women's Hospitals 4 1 0 0 0 0 0 5
Developmental Genetics Unit,King Faisal Specialist Hospital & Research Centre 0 5 0 0 0 0 0 5
UCLA Clinical Genomics Center, UCLA 1 4 0 0 0 0 0 5
Undiagnosed Diseases Network,NIH 2 3 0 0 0 0 0 5
ClinVar Staff, National Center for Biotechnology Information (NCBI) 0 4 0 0 0 0 0 4
Dobyns Lab,Seattle Children's Research Institute 2 1 1 0 0 0 0 4
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille 3 1 0 0 0 0 0 4
Center for Human Genetics and Laboratory Diagnostics, Dr. Klein, Dr. Rost and Colleagues 0 2 2 0 0 0 0 4
Clinical Genetics Group,University of Otago 4 0 0 0 0 0 0 4
Epi4K Consortium 0 4 0 0 0 0 0 4
Clinical Genetics laboratory, University of Goettingen 1 1 1 0 0 0 0 3
Institute of Human Genetics,Cologne University 0 0 2 1 0 0 0 3
Centogene AG - the Rare Disease Company 1 2 0 0 0 0 0 3
Division of Human Genetics,Children's Hospital of Philadelphia 0 1 2 0 0 0 0 3
Knight Diagnostic Laboratories, Oregon Health and Sciences University 1 1 1 0 0 0 0 3
Soonchunhyang University Bucheon Hospital,Soonchunhyang University Medical Center 1 0 1 1 0 0 0 3
Geisinger Autism and Developmental Medicine Institute,Geisinger Health System 1 0 2 0 0 0 0 3
Department of Genetics,Sultan Qaboos University Hospital, Oman 3 0 0 0 0 0 0 3
UNC Molecular Genetics Laboratory,University of North Carolina at Chapel Hill 0 0 3 0 0 0 0 3
Cavalleri Lab, Royal College of Surgeons in Ireland 1 2 0 0 0 0 0 3
Pathology and Clinical Laboratory Medicine,King Fahad Medical City 2 0 0 0 1 0 0 3
Johns Hopkins Genomics, Johns Hopkins University 0 1 2 0 0 0 0 3
deCODE genetics, Amgen 0 0 0 0 0 3 0 3
Center for Reproductive Medicine, Peking University Third Hospital 0 1 2 0 0 0 0 3
Nilou-Genome Lab 0 0 0 1 2 0 0 3
Engle Laboratory,Boston Children's Hospital 1 1 0 0 0 0 0 2
Victorian Clinical Genetics Services,Murdoch Childrens Research Institute 0 1 1 0 0 0 0 2
Institute of Human Genetics,Friedrich-Alexander-Universität Erlangen-Nürnberg 2 0 0 0 0 0 0 2
Center of Genomic medicine, Geneva,University Hospital of Geneva 2 0 0 0 0 0 0 2
Diagnostics Division,Centre for DNA Fingerprinting and Diagnostics 0 2 0 0 0 0 0 2
Genetic Diagnostic Laboratory,University of Szeged 1 1 0 0 0 0 0 2
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 1 0 1 0 0 0 0 2
NIHR Bioresource Rare Diseases, University of Cambridge 1 1 0 0 0 0 0 2
Heinzen Lab,Columbia University 2 0 0 0 0 0 0 2
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 0 2 0 0 0 0 0 2
Ege University Pediatric Genetics,Ege University 2 0 0 0 0 0 0 2
SIB Swiss Institute of Bioinformatics 1 0 0 0 1 0 0 2
Department of Pathology and Laboratory Medicine,Sinai Health System 0 0 1 1 0 0 0 2
CHLA Center for Personalized Medicine,Children's Hospital, Los Angeles 1 0 1 0 0 0 0 2
Institute for Genomic Medicine, Nationwide Children's Hospital 2 0 0 0 0 0 0 2
Genome Diagnostics Laboratory,VU University Medical Center Amsterdam 2 0 0 0 0 0 0 2
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center 0 1 0 0 1 0 0 2
Consultorio y Laboratorio de Neurogenética,Hospital JM Ramos Mejia 0 2 0 0 0 0 0 2
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota 1 1 0 0 0 0 0 2
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 1 1 0 0 0 0 0 2
Institute for Genomic Medicine (IGM) Clinical Laboratory,Nationwide Children's Hospital 0 1 1 0 0 0 0 2
Breda Genetics srl 0 0 2 0 0 0 0 2
Cytogenetics and Genomics Lab,Cyprus Institute Of Neurology and Genetics 1 1 0 0 0 0 0 2
Clinical Genomics Program, Stanford Medicine 0 0 2 0 0 0 0 2
UOSD Laboratory of Genetics & Genomics of Rare Diseases,Istituto Giannina Gaslini 0 1 1 0 0 0 0 2
Medical Genetics Laboratory,CHRU Nancy 2 0 0 0 0 0 0 2
Clinical Molecular Genetics Laboratory,Johns Hopkins All Children's Hospital 1 0 0 0 0 0 0 1
Courtagen Diagnostics Laboratory,Courtagen Life Sciences 1 0 0 0 0 0 0 1
Blueprint Genetics 0 1 0 0 0 0 0 1
CSER _CC_NCGL, University of Washington 0 0 0 1 0 0 0 1
Prenatal Medicine Munich,Prenatal Medicine Munich 0 1 0 0 0 0 0 1
Center for Human Genetics,University of Leuven 1 0 0 0 0 0 0 1
Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin 0 0 1 0 0 0 0 1
Laboratory Genomica,Gynecology and Assisted Reproduction Hospital Malinov DM 1 0 0 0 0 0 0 1
Bioinformatics dept.,Datar Cancer Genetics Limited, India 0 0 1 0 0 0 0 1
Reutter Lab, Institute of Human Genetics, University Hospital Bonn 1 0 0 0 0 0 0 1
Research Group Niklas Dahl,Uppsala University 1 0 0 0 0 0 0 1
Talkowski Laboratory, Center for Human Genetic Research,Massachusetts General Hospital 0 0 1 0 0 0 0 1
Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences 1 0 0 0 0 0 0 1
Neurogenetics Laboratory - MEYER,AOU Meyer 0 0 1 0 0 0 0 1
Phosphorus, Inc. 0 0 1 0 0 0 0 1
Rare Disease Group, Clinical Genetics,Karolinska Institutet 0 1 0 0 0 0 0 1
Genetics Department, University Hospital of Toulouse 0 0 1 0 0 0 0 1
Genetics Division,Universidade Federal de Sao Paulo 0 1 0 0 0 0 0 1
Variantyx, Inc. 0 1 0 0 0 0 0 1
Laboratory of Medical Genetics, University of Torino 1 0 0 0 0 0 0 1
Department of Pediatrics,Driscoll Children's Hospital 1 0 0 0 0 0 0 1
Pediatric Neurology,Northwest Women’s and Children’s Hospital 1 0 0 0 0 0 0 1
Clinical Genetics Laboratory,Federal University of Health Sciences of Porto Alegre 0 1 0 0 0 0 0 1
Molecular Genetics Center,Sichuan Provincial People's Hospital 0 1 0 0 0 0 0 1
Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine 1 0 0 0 0 0 0 1
Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn 1 0 0 0 0 0 0 1
Reproductive Health Research and Development,BGI Genomics 1 0 0 0 0 0 0 1
Myelin Disorders Clinic-Children's Medical Center/Medical Genetics Lab-Tarbiat Modares University, Children's Medical Center, Pediatrics Center of Excellence, 0 0 1 0 0 0 0 1
SavaGenome Genetic Health Clinic 1 0 0 0 0 0 0 1
Institut de Recherche Interdisciplinaire en Biologie Humaine et Moleculaire,Universite Libre de Bruxelles 1 0 0 0 0 0 0 1
GenomeConnect - CFC International 0 0 0 0 0 0 1 1
Myriad Women's Health, Inc. 1 0 0 0 0 0 0 1
Clinical Genetics Laboratory, Skane University Hospital Lund 0 1 0 0 0 0 0 1
Department of Molecular Bıology and Genetics,Istanbul Technical University 0 1 0 0 0 0 0 1
Pars Genome Lab 0 0 1 0 0 0 0 1
Comprehensive Medical Genetic Center, Shiraz University of Medical Sciences 1 0 0 0 0 0 0 1
Sezerman Lab, Dept of Biostatistics and Bioinformatics, Acibadem Mehmet Ali Aydinlar University 0 1 0 0 0 0 0 1

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