ClinVar Miner

Variants studied for thoracic malformation

Included ClinVar conditions (76):
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 not provided total
1825 1120 7830 9295 1148 25 20051

Gene and significance breakdown #

Total genes and gene combinations: 167
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
DYNC2H1 357 250 694 1787 149 1 2920
EVC2 203 128 362 933 72 0 1614
EVC 166 129 417 861 112 0 1579
KIAA0586 83 34 587 407 56 2 1166
TTC21B 72 37 520 423 55 0 1033
WDR19 66 40 490 387 41 2 964
IFT172 43 28 459 421 26 0 952
IFT140 54 23 471 456 48 1 951
DOK7 71 56 293 465 42 2 907
CSPP1 77 22 422 277 33 1 826
MUSK 45 23 231 331 42 3 665
RAPSN 77 45 186 331 18 1 620
IFT80, TRIM59-IFT80 42 17 309 205 34 1 572
NEK1 48 31 287 202 42 0 559
IFT122 36 16 250 233 42 5 537
IFT140, LOC105371046 39 19 251 236 29 0 523
WDR35 37 18 260 160 54 1 492
DYNC2I1 20 9 145 169 41 1 377
TCTN3 30 8 171 144 13 0 364
CEP120 17 10 131 143 36 0 334
DYNC2I2 25 10 127 125 17 0 296
ARFGEF1, CSPP1 8 5 103 66 10 0 190
IFT172, KRTCAP3 11 7 74 68 7 1 160
IFT140, LOC126862260 6 6 69 77 5 0 154
STRA6 24 3 66 36 29 0 146
IFT172, LOC126806173 9 3 68 56 5 1 138
DYNC2I2, LOC126860772 11 4 70 47 7 0 134
EVC2, LOC126806961 11 12 33 63 11 0 123
IFT172, LOC126806174 6 2 30 40 2 0 77
LOC130004408, TCTN3 7 1 22 26 4 0 60
DOK7, LOC129992118 3 3 24 25 3 0 57
RARB 6 11 18 10 9 0 51
IFT43 3 5 25 12 3 1 44
DOK7, LOC126806951 1 3 11 18 2 0 35
GLE1, LOC101929270 1 0 23 3 6 0 33
GLE1 1 1 21 3 5 0 29
EVC, LOC129992144 6 11 5 6 0 0 25
KIAA0753 6 2 0 3 9 0 19
DYNC2LI1 11 2 5 0 1 0 18
EVC2, LOC126806962 0 1 3 12 0 0 16
EVC, EVC2 9 0 2 4 3 0 15
IFT122, LOC126806810 0 1 6 8 2 0 14
NUP88 3 0 3 0 6 0 12
IFT80 5 1 5 0 0 0 11
IFT81 7 6 3 0 0 0 11
RYR1 4 7 0 0 0 0 11
IFT52 6 3 3 0 1 0 10
INTU 2 4 2 2 2 0 9
NEK9 1 2 2 1 3 0 9
LOC129933186, WDR35 0 0 4 2 1 0 7
IFT122, LOC129937552 1 0 3 2 1 1 6
DYNC2I1, LOC129999765 0 0 1 4 0 0 5
TRAF3IP1 4 4 1 0 0 0 5
ABCG5, DYNC2LI1 1 2 1 0 0 0 4
DYNC1H1 0 1 3 0 0 0 4
DYNLT2B, TM4SF19-DYNLT2B 2 0 1 0 1 0 4
LOC129993365, NEK1 0 0 3 1 0 0 4
DOK7, LOC126806951, LOC129992118 3 0 0 0 0 0 3
DYNLT2B 2 1 0 0 0 0 3
GLDN 0 3 1 0 0 0 3
GLE1, LOC130002710 0 0 3 0 0 0 3
GRK2 1 2 0 0 0 0 3
IFT74 0 3 2 0 0 0 3
NALCN 0 3 0 0 0 0 3
PIEZO2 2 1 0 0 0 0 3
WNT7B 3 0 0 0 0 0 3
ACTA1 1 1 0 0 0 0 2
ASAH1 0 2 0 0 0 0 2
ASPM 1 1 0 0 0 0 2
BLTP1 0 2 0 0 0 0 2
C2CD3 0 0 2 0 0 0 2
CBR4, NEK1, PALLD, SH3RF1 1 0 1 0 0 0 2
CILK1 1 1 0 0 0 0 2
DYNC2I2, LOC126860772, SPTAN1 1 0 1 0 0 0 2
DYNC2I2, SPTAN1 1 1 1 0 0 0 2
EARS2 0 2 0 0 0 0 2
EVC, LOC129992148 0 0 1 1 0 0 2
FUZ 1 2 1 0 0 0 2
IFT43, TGFB3 0 0 0 2 0 0 2
INTU, LOC126807151 0 2 1 0 0 0 2
LBR 2 2 0 0 0 0 2
LGI4 0 2 0 0 0 0 2
LOC126862474, NUP88 0 0 1 0 1 0 2
LOC129993367, NEK1 0 0 0 0 2 0 2
MATN3, WDR35, WDR35-DT 0 0 0 0 2 0 2
RAB34 0 2 0 0 0 0 2
ROR2 0 2 0 0 0 0 2
SPAG16 0 0 2 0 0 0 2
VPS13D 0 0 2 0 0 0 2
ABCA3, ADCY9, AMDHD2, ANKS3, ANTKMT, ARHGDIG, ATP6V0C, AXIN1, BAIAP3, BICDL2, BRICD5, C16orf90, C16orf96, C1QTNF8, CACNA1H, CAPN15, CASKIN1, CCDC154, CCDC78, CCNF, CDIP1, CEMP1, CHTF18, CIAO3, CLCN7, CLDN6, CLDN9, CLUAP1, CORO7, CORO7-PAM16, CRAMP1, CREBBP, DECR2, DNAAF8, DNAJA3, DNASE1, DNASE1L2, E4F1, ECI1, ELOB, EME2, FAHD1, FAM234A, FBXL16, FLYWCH1, FLYWCH2, GFER, GLIS2, GNG13, GNPTG, HAGH, HAGHL, HCFC1R1, HMOX2, HS3ST6, IFT140, IGFALS, IL32, JMJD8, JPT2, KCTD5, KREMEN2, LMF1, LUC7L, MAPK8IP3, MCRIP2, MEFV, MEIOB, METRN, METTL26, MGRN1, MIR1225, MLST8, MMP25, MRPL28, MRPS34, MSLN, MSRB1, MTRNR2L4, NAA60, NDUFB10, NHERF2, NHLRC4, NLRC3, NME3, NME4, NMRAL1, NOXO1, NPW, NTHL1, NTN3, NUBP2, NUDT16L1, OR1F1, OR2C1, PAM16, PAQR4, PDIA2, PDPK1, PGAP6, PGP, PIGQ, PKD1, PKMYT1, PRR25, PRR35, PRSS21, PRSS22, PRSS27, PRSS33, PRSS41, PTX4, RAB11FIP3, RAB26, RAB40C, RGS11, RHBDL1, RHOT2, RNF151, RNPS1, ROGDI, RPL3L, RPS2, RPUSD1, SEPTIN12, SLX4, SMIM22, SNHG9, SOX8, SPSB3, SRL, SRRM2, SSTR5, STUB1, SYNGR3, TBC1D24, TBL3, TEDC2, TELO2, TFAP4, THOC6, TIGD7, TMEM204, TNFRSF12A, TPSAB1, TPSB2, TPSD1, TPSG1, TRAF7, TRAP1, TSC2, TSR3, UBALD1, UBE2I, UNKL, UQCC4, VASN, WDR24, WDR90, WFIKKN1, ZG16B, ZNF174, ZNF200, ZNF205, ZNF213, ZNF263, ZNF500, ZNF597, ZNF598, ZNF75A, ZSCAN10, ZSCAN32 0 0 1 0 0 0 1
ACP2, ARFGAP2, CSTPP1, DDB2, LRP4, MADD, MYBPC3, NR1H3, PACSIN3, PSMC3, RAPSN, SLC39A13, SPI1 1 0 0 0 0 0 1
ADD1, ADRA2C, CYTL1, DOK7, EVC2, FAM193A, GRK4, HAUS3, HGFAC, HTT, LINC01587, LRPAP1, LYAR, MFSD10, MSANTD1, MSX1, MXD4, NOP14, NSG1, OTOP1, POLN, RGS12, RNF4, SH3BP2, STK32B, STX18, TMEM128, TNIP2, ZBTB49, ZFYVE28 1 0 0 0 0 0 1
ADD1, DOK7, GRK4, HGFAC, HTT, MFSD10, MSANTD1, NOP14, RGS12, SH3BP2 1 0 0 0 0 0 1
ADSS1 1 0 0 0 0 0 1
ALDH5A1 0 1 0 0 0 0 1
ALOXE3, HES7, LOC126862485, LOC130060199, LOC130060200, LOC130060201, LOC130060202, LOC130060203, LOC130060204, LOC130060205, LOC130060206, TRG-GCC2-6, TRK-TTT3-5, TRL-TAG1-1, TRQ-CTG1-5, TRR-TCT2-1 1 0 0 0 0 0 1
ANGPTL5, BIRC2, BIRC3, CEP126, CFAP300, DCUN1D5, DYNC2H1, MMP1, MMP10, MMP12, MMP13, MMP20, MMP27, MMP3, MMP7, MMP8, TMEM123, TRPC6, YAP1 1 0 0 0 0 0 1
ANTKMT, ARHGDIG, AXIN1, BAIAP3, C1QTNF8, CACNA1H, CAPN15, CCDC154, CCDC78, CHTF18, CIAO3, CLCN7, DECR2, FAM234A, FBXL16, GNG13, GNPTG, HAGHL, IFT140, JMJD8, LMF1, LUC7L, MCRIP2, METRN, METTL26, MRPL28, MSLN, NHLRC4, NME4, PDIA2, PGAP6, PIGQ, PRR25, PRR35, PTX4, RAB11FIP3, RAB40C, RGS11, RHBDL1, RHOT2, RPUSD1, SOX8, SSTR5, STUB1, TELO2, TMEM204, TPSAB1, TPSB2, TPSD1, TPSG1, TSR3, UBE2I, UNKL, UQCC4, WDR24, WDR90, WFIKKN1 1 0 0 0 0 0 1
ARFGEF1, COPS5, CSPP1, MCMDC2, PPP1R42, SNHG6, SNORD87, TCF24 0 0 1 0 0 0 1
ARFGEF1, CPA6, CSPP1 1 0 0 0 0 0 1
ARID4A, KIAA0586, PSMA3, TIMM9, TOMM20L 1 0 0 0 0 0 1
ASCC1 1 0 0 0 0 0 1
ATP2B3 0 1 0 0 0 0 1
AVEN, RYR3 0 0 1 0 0 0 1
B9D1 0 0 1 0 0 0 1
BBS10 1 0 0 0 0 0 1
CACNG2-DT, IFT27 1 0 0 0 0 0 1
CACNG2-DT, IFT27, LOC126863139 1 0 0 0 0 0 1
CCDC39 0 0 1 0 0 0 1
CHRND 0 1 0 0 0 0 1
CHRNG 0 1 0 0 0 0 1
CLCN7, IFT140, PTX4, TELO2 0 0 1 0 0 0 1
CNTNAP1 0 1 0 0 0 0 1
CNTNAP1, LOC125177481 1 0 0 0 0 0 1
COPS5, CSPP1, PPP1R42 0 0 1 0 0 0 1
CSRNP3, GALNT3, SCN1A, SCN2A, SCN3A, SCN9A, TTC21B 1 0 0 0 0 0 1
DOCK7 0 1 0 0 0 0 1
DQX1 0 0 1 0 0 0 1
DYNLT2B, LOC129938285, TM4SF19-DYNLT2B 0 0 1 0 0 0 1
ENTPD1, TCTN3 0 0 1 0 0 0 1
ERBB3 0 0 1 0 0 0 1
EVC2, LINC01587, STK32B 1 0 0 0 0 0 1
EXOSC3 1 0 0 0 0 0 1
FAM98C 0 1 0 0 0 0 1
FBLN1 0 0 1 0 0 0 1
FBN2 0 1 0 0 0 0 1
FLVCR1 0 1 0 0 0 0 1
FLVCR1, LOC129932486 0 1 0 0 0 0 1
FNDC4, GCKR, IFT172 0 0 1 0 0 0 1
GBE1 0 1 0 0 0 0 1
GCN1 0 0 1 0 0 0 1
GFRA4 0 0 1 0 0 0 1
IFT122, MBD4 0 0 1 0 0 0 1
IFT122, MBD4, RHO 0 0 1 0 0 0 1
IFT140, PTX4, TELO2 0 0 1 0 0 0 1
IFT140, TELO2 1 0 0 0 0 0 1
IFT140, TMEM204 0 0 1 0 0 0 1
IFT88 0 1 1 0 0 0 1
INTU, LOC123480930 1 0 0 0 0 0 1
IQSEC3 0 0 1 0 0 0 1
IQSEC3, LOC574538 0 0 1 0 0 0 1
KIF24 1 0 0 0 0 0 1
LOC112939934, WDR19 0 0 1 0 0 0 1
LOC124310625, LOC126860730, MUSK 1 0 0 0 0 0 1
LOC124310625, MUSK 0 1 0 0 0 0 1
LOC129935046, TTC21B 0 0 0 0 1 0 1
LOC129993366, NEK1 0 0 1 0 0 0 1
MAGI3 0 0 1 0 0 0 1
MATN3, WDR35 0 0 0 1 1 0 1
MUSK, SVEP1, TXN, TXNDC8 0 0 1 0 0 0 1
NAGA 0 0 1 0 0 0 1
NGLY1, RARB, TOP2B 0 0 1 0 0 0 1
NUP88, RABEP1 0 0 0 0 1 0 1
PRG4 0 0 1 0 0 0 1
PRICKLE1 0 0 1 0 0 0 1
PSMC3, RAPSN, SLC39A13 0 0 1 0 0 0 1
SCN4A 0 1 0 0 0 0 1
SCN5A 0 1 0 0 0 0 1
SCN8A 0 1 0 0 0 0 1
SETBP1 1 0 0 0 0 0 1
SLTM 0 1 0 0 0 0 1
SPAG17 0 1 0 0 0 0 1
TMEM256, TMEM256-PLSCR3 0 1 0 0 0 0 1
TMPO 0 0 1 0 0 0 1
UNC50 0 0 1 0 0 0 1
ZEB2 0 0 1 0 0 0 1
ZNF875 0 0 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 134
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 1437 433 6340 9037 974 0 18221
Illumina Laboratory Services, Illumina 0 2 1233 195 329 0 1717
Fulgent Genetics, Fulgent Genetics 39 56 604 247 17 0 963
University of Washington Center for Mendelian Genomics, University of Washington 1 233 0 0 0 0 234
Dan Cohn Lab, University Of California Los Angeles 183 10 20 0 0 0 212
Baylor Genetics 57 83 64 0 0 0 200
OMIM 196 0 1 0 0 0 197
Genome-Nilou Lab 0 3 7 3 157 0 170
Counsyl 18 80 55 2 0 0 155
Natera, Inc. 15 3 61 32 31 0 142
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 3 5 37 23 44 0 112
Myriad Genetics, Inc. 1 91 1 0 0 0 93
Revvity Omics, Revvity 16 10 50 1 0 0 77
Cirak Lab, University Hospital Cologne 13 33 22 0 0 0 68
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 14 22 17 0 0 0 52
Rare Disease Group, Clinical Genetics, Karolinska Institutet 15 10 23 0 0 0 48
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 23 11 0 0 0 0 34
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 7 9 15 0 0 0 31
Juno Genomics, Hangzhou Juno Genomics, Inc 8 10 13 0 0 0 31
Pars Genome Lab 0 0 0 1 28 0 29
Mendelics 9 6 2 0 11 0 28
Neuberg Centre For Genomic Medicine, NCGM 2 11 13 0 0 0 26
3billion 5 5 5 8 0 0 23
New York Genome Center 2 3 15 0 0 0 20
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center 0 0 0 4 15 0 19
UW Hindbrain Malformation Research Program, University of Washington 17 0 0 0 0 0 17
Centre for Mendelian Genomics, University Medical Centre Ljubljana 3 5 7 0 1 0 16
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ 6 2 4 0 0 0 12
GeneReviews 0 0 0 0 0 11 11
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India 7 2 2 0 0 0 11
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 4 7 0 0 0 0 11
SIB Swiss Institute of Bioinformatics 1 9 1 0 0 0 11
Laboratory of Medical Genetics (UMR_S 1112), INSERM/Strasbourg University 11 0 0 0 0 0 11
Laboratory of Inherited Metabolic Diseases, Research centre for medical genetics 4 3 4 0 0 0 11
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 10 10
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine 3 6 0 0 0 0 9
Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital 3 3 2 0 0 0 8
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München 4 4 0 0 0 0 8
Genomic Research Center, Shahid Beheshti University of Medical Sciences 1 2 4 1 0 0 8
Institute of Human Genetics, University of Leipzig Medical Center 1 1 5 1 0 0 8
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 0 0 8 0 8
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 1 3 3 0 0 0 7
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard 1 2 3 0 0 0 6
Molecular Biology Laboratory, Fundació Puigvert 4 2 0 0 0 0 6
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 2 2 2 0 0 0 6
David Geffen School of Medicine, University of California, Los Angeles 5 0 0 0 0 0 5
Diagnostics Division, CENTRE FOR DNA FINGERPRINTING AND DIAGNOSTICS 4 1 0 0 0 0 5
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City 1 4 0 0 0 0 5
Genomic Medicine Lab, University of California San Francisco 3 1 1 0 0 0 5
Johns Hopkins Genomics, Johns Hopkins University 0 2 3 0 0 0 5
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital 0 1 1 0 3 0 5
Molecular Genetics, Royal Melbourne Hospital 0 2 1 1 1 0 5
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 3 1 0 0 0 0 4
Genetic Services Laboratory, University of Chicago 2 2 0 0 0 0 4
Genome Diagnostics Laboratory, University Medical Center Utrecht 0 0 0 1 3 0 4
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 1 2 1 0 0 0 4
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare 2 1 1 0 0 0 4
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues 1 3 0 0 0 0 4
Genetics and Molecular Pathology, SA Pathology 0 3 1 0 0 0 4
GenomeConnect, ClinGen 0 0 0 0 0 4 4
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 2 2 0 0 0 0 4
MVZ Medizinische Genetik Mainz 0 2 2 0 0 0 4
Institute of Human Genetics, Cologne University 0 2 1 0 0 0 3
MGZ Medical Genetics Center 0 1 2 0 0 0 3
Centogene AG - the Rare Disease Company 1 1 1 0 0 0 3
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 3 0 0 0 0 0 3
Reproductive Health Research and Development, BGI Genomics 1 0 2 0 0 0 3
Pediatrics Genetics, Post Graduate Institute of Medical Education and Research 1 2 0 0 0 0 3
Division of Genetics, Dept of Pediatrics, All India Institute of Medical Sciences 2 1 0 0 0 0 3
DASA 2 1 0 0 0 0 3
Mayo Clinic Laboratories, Mayo Clinic 0 0 2 0 0 0 2
CHU Sainte-Justine Research Center, University of Montreal 0 2 0 0 0 0 2
Care4Rare-SOLVE, CHEO 0 2 0 0 0 0 2
Department Of Medical Genetics, Faculty Of Medicine, Ege University 0 2 0 0 0 0 2
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine 0 0 2 0 0 0 2
Center of Genomic medicine, Geneva, University Hospital of Geneva 1 1 0 0 0 0 2
Centre for Genomic and Experimental Medicine, University of Edinburgh 2 0 0 0 0 0 2
Soonchunhyang University Bucheon Hospital, Soonchunhyang University Medical Center 0 2 0 0 0 0 2
Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences 0 2 0 0 0 0 2
Yale Center for Mendelian Genomics, Yale University 2 0 0 0 0 0 2
Laboratorio de Citogenómica y Microarreglos, Universidad Autonoma de Nuevo Leon 0 2 0 0 0 0 2
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 1 0 1 0 0 0 2
Pediatric Genomics Discovery Program, Yale University 0 2 0 0 0 0 2
Cancer Diagnostics Division, Gene Solutions 2 0 0 0 0 0 2
UNC Molecular Genetics Laboratory, University of North Carolina at Chapel Hill 0 2 0 0 0 0 2
Hainan Provincial Key Laboratory for Human Reproductive Medicine and Genetic Research 1 0 1 0 0 0 2
Istanbul Faculty of Medicine, Istanbul University 2 0 0 0 0 0 2
Molecular Genetics laboratory, Necker Hospital 2 0 0 0 0 0 2
Fundación para la Investigación Sanitaria y Biomédica de la Comunidad Valenciana, FISABIO Oftalmología Médica 2 0 0 0 0 0 2
Precision Medical Center, Maternal and Child Health Hospital of Hubei Province 0 0 2 0 0 0 2
Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn 0 1 1 0 0 0 2
Suma Genomics 1 0 1 0 0 0 2
Genomics England Pilot Project, Genomics England 0 2 0 0 0 0 2
Hôpital Purpan 2 0 0 0 0 0 2
Eurofins-Biomnis 1 1 0 0 0 0 2
Clinical Laboratory Sciences Program (CLSP), King Saud bin Abdulaziz University for Health Sciences (KSAU-HS) 0 1 0 1 0 0 2
Medical Genetics Center, Maternal and Child Health Hospital of Hubei Province 0 2 0 0 0 0 2
Solve-RD Consortium 0 2 0 0 0 0 2
Prenatal Diagnosis Center, International Peace Maternity & Child Health Hospital 2 0 0 0 0 0 2
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet 0 0 1 0 0 0 1
Institute for Genomic Medicine (IGM) Clinical Laboratory, Nationwide Children's Hospital 1 0 0 0 0 0 1
Human Developmental Genetics Laboratory, Medical College of Wisconsin 0 0 1 0 0 0 1
Intergen, Intergen Genetics and Rare Diseases Diagnosis Center 1 0 0 0 0 0 1
UCLA Clinical Genomics Center, UCLA 0 1 0 0 0 0 1
Department of Medical Genetics, Oslo University Hospital 0 1 0 0 0 0 1
Clinical Genetics and Genomics, Karolinska University Hospital 0 0 1 0 0 0 1
Institute for Human Genetics and Genomic Medicine, Uniklinik RWTH Aachen 0 0 1 0 0 0 1
Harry Perkins Institute Of Medical Research, University Of Western Australia 0 1 0 0 0 0 1
Division of Human Genetics, Children's Hospital of Philadelphia 1 0 0 0 0 0 1
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 0 0 1 0 0 1
Paul Sabatier University EA-4555, Paul Sabatier University 1 0 0 0 0 0 1
Centre for Genomic Medicine, Manchester, Central Manchester University Hospitals 1 0 0 0 0 0 1
Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin 0 0 1 0 0 0 1
Center for Statistical Genetics, Columbia University 1 0 0 0 0 0 1
Daryl Scott Lab, Baylor College of Medicine 0 1 0 0 0 0 1
Center for Molecular Medicine, Children’s Hospital of Fudan University 1 0 0 0 0 0 1
Ege University Pediatric Genetics, Ege University 1 0 0 0 0 0 1
Geisinger Autism and Developmental Medicine Institute, Geisinger Health System 0 0 1 0 0 0 1
Genetics Department, University Hospital of Toulouse 0 1 0 0 0 0 1
Cormier-Daire Lab, IMAGINE 1 0 0 0 0 0 1
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota 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 1
Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn 0 1 0 0 0 0 1
MedGen Diagnostic Laboratory, MedGen Medical Centre 1 0 0 0 0 0 1
Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center 1 0 0 0 0 0 1
MNM Diagnostics 1 0 0 0 0 0 1
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ 0 0 1 0 0 0 1
Lifecell International Pvt. Ltd 1 0 0 0 0 0 1
Pediatric Genetics Clinic, Sheba Medical Center 1 0 0 0 0 0 1
Genetic Diagnostics Department, Viafet Genomics Laboratory 0 1 0 0 0 0 1
Department of Human Genetics, Hannover Medical School 1 0 0 0 0 0 1
Pediatric/Medical Genetics, Ministry of Health, Qatif Central Hospital 1 0 0 0 0 0 1
Medical Genetics Laboratory, Etlik City Hospital 1 0 0 0 0 0 1
Royal Medical Services, Bahrain Defence Force Hospital 0 0 1 0 0 0 1

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