ClinVar Miner

Variants studied for cranial nerve neuropathy

Included ClinVar conditions (169):
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
610 415 2498 806 1077 2 25 5127

Gene and significance breakdown #

Total genes and gene combinations: 196
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign risk factor not provided total
ATP7B 229 228 413 268 53 0 12 982
LRPPRC 8 42 189 24 29 0 1 279
MT-ND5 11 3 113 48 104 0 0 273
MT-CYB 4 0 122 36 94 0 0 252
OPA3 6 4 122 31 79 0 1 243
MT-ATP6 12 5 85 47 92 0 1 238
OPA1 31 12 64 16 40 0 3 160
MT-ND2 4 1 62 42 51 0 0 158
MT-CO1 0 1 87 20 47 0 0 155
NDUFA10 0 0 115 11 29 0 0 154
MT-CO3 4 0 69 29 40 0 0 140
MT-ND1 16 2 55 23 52 0 0 140
KIF21A 8 0 53 9 55 0 0 125
MT-ND4 5 1 55 20 38 0 1 116
SURF1 29 11 52 19 11 0 1 109
SDHA 1 1 61 10 20 0 1 94
MT-ND6 11 1 34 16 33 1 1 92
MT-CO2 0 0 44 18 25 0 0 87
COX10 0 0 51 10 25 0 0 86
NDUFS1 0 3 52 10 15 0 0 80
DLD 0 0 48 5 19 0 0 72
COX15 0 1 62 4 3 0 0 70
CHN1 10 0 44 5 4 0 1 64
MT-ATP8 0 1 22 7 28 0 0 58
FRMD7 13 1 23 5 12 0 0 54
NDUFV1 2 3 42 2 4 0 0 52
ECHS1 21 17 8 0 0 0 0 41
MT-ND3 6 0 17 7 12 0 0 41
SCO1 0 0 30 2 7 0 0 39
COX15, ENTPD7 0 0 28 4 3 0 0 35
NDUFS4 5 1 18 2 5 0 1 31
NDUFAF5 0 3 22 1 3 0 0 29
BCS1L 3 1 18 1 3 0 0 26
MT-ND4L 1 0 12 6 7 0 0 26
NDUFS8 0 3 21 0 1 0 0 25
MT-ATP6, MT-ATP8 0 0 3 8 13 0 0 24
NDUFS3 0 0 23 0 0 0 0 23
NDUFS7 0 0 18 0 2 0 0 20
​intergenic 8 2 9 0 0 0 0 19
NDUFAF2 2 1 13 1 2 0 0 19
TMEM126A 1 0 9 6 4 0 0 19
ATP1A3 7 6 3 0 0 0 0 16
COQ2 5 3 7 0 2 0 0 15
AFG3L2 12 0 1 0 0 0 0 13
TUBB3 11 1 2 0 0 0 0 13
COX15, CUTC 0 0 10 0 2 0 0 12
FOXRED1 3 1 6 0 0 0 0 10
LOC112529895, SCO1 0 0 9 1 0 0 0 10
MAPT 7 0 3 0 0 0 0 10
PDSS2 2 0 6 0 0 0 0 8
RTN4IP1 5 1 2 0 0 0 0 8
GAMT, NDUFS7 0 0 0 7 0 0 0 7
GPR143 4 1 1 0 0 0 0 6
MECR 0 6 0 0 0 0 0 6
NDUFAF6 2 1 3 0 0 0 0 6
NF1 5 0 1 0 0 0 0 6
ACO2, POLR3H 3 0 2 0 0 0 0 5
COQ8A 0 3 2 0 0 0 0 5
COX10, LOC105943586 0 0 2 1 2 0 0 5
ACO2 1 0 4 0 0 0 0 4
ALG11, ATP7B, UTP14C 4 0 0 0 0 0 0 4
COQ2, LOC112997540 0 0 3 0 1 0 0 4
DNM1L 3 0 1 0 0 0 0 4
ERCC8, NDUFAF2 0 0 1 1 2 0 0 4
GNB1 4 0 0 0 0 0 0 4
MAFB 4 0 0 0 0 0 0 4
SSBP1 4 0 0 0 0 0 0 4
TMEM67 1 3 0 0 0 0 0 4
TYR 3 1 0 0 0 0 0 4
COL25A1 3 0 0 0 0 0 0 3
FASTKD2 3 0 0 0 0 0 0 3
HECW2 0 0 0 3 0 0 0 3
LOC112081413, NDUFS8 0 0 2 0 1 0 0 3
LOC113788297, NDUFAF6 0 0 3 0 0 0 0 3
MT-TW 3 0 0 0 0 0 0 3
PHOX2A 3 0 0 0 0 0 0 3
SLC52A3 1 1 1 0 0 0 0 3
TUBA1A 1 2 0 0 0 0 0 3
ALG11, ATP7B 0 0 1 1 1 0 0 2
CASK 0 2 0 0 0 0 0 2
CDH11 0 0 0 2 0 0 0 2
CEP290 2 0 0 0 0 0 0 2
DHX30 2 0 0 0 0 0 0 2
DNM1L, YARS2 1 1 0 0 0 0 0 2
FAM71A 0 0 0 2 0 0 0 2
GALC 0 2 0 0 0 0 0 2
GUCY2D 0 1 1 0 0 0 0 2
HARS1 2 0 0 0 0 0 0 2
IARS2 2 0 0 0 0 0 0 2
KBTBD7, LOC101929140 0 0 0 2 0 0 0 2
MED13L 2 0 0 0 0 0 0 2
MKS1 2 0 0 0 0 0 0 2
MRPL28 0 0 0 2 0 0 0 2
MT-TK 2 0 0 0 0 0 0 2
MT-TL1 1 0 1 0 0 0 0 2
MT-TV 2 0 0 0 0 0 0 2
NDUFA12 0 0 2 0 0 0 0 2
NDUFA13 2 0 0 0 0 0 0 2
NDUFA9 0 0 2 0 0 0 0 2
NDUFS8, TCIRG1 0 0 1 1 0 0 0 2
PLCB2 0 0 0 2 0 0 0 2
PMPCA 2 0 0 0 0 0 0 2
PTCH2 0 0 0 2 0 0 0 2
QARS1 0 2 0 0 0 0 0 2
RUBCN 2 0 0 0 0 0 0 2
SGSH 2 0 0 0 0 0 0 2
SIM1 0 0 0 2 0 0 0 2
SLC9A6 0 1 1 0 0 0 0 2
YME1L1 1 0 1 0 0 0 0 2
ABCG4, ACRV1, ADAMTS15, ADAMTS8, APLP2, APOA1, APOA4, APOA5, APOC3, ARCN1, ARHGAP32, ARHGEF12, ATP5MG, BACE1, BARX2, BCL9L, BLID, BSX, BUD13, C11orf45, C1QTNF5, C2CD2L, CADM1, CBL, CCDC15, CCDC153, CD3D, CD3E, CD3G, CDON, CENATAC, CEP164, CHEK1, CLMP, CRTAM, CXCR5, DCPS, DDX25, DDX6, DPAGT1, DSCAML1, EI24, ESAM, ETS1, FAM118B, FEZ1, FLI1, FOXR1, FOXRED1, FXYD2, FXYD6, FXYD6-FXYD2, GRAMD1B, GRIK4, H2AX, HEPACAM, HEPN1, HINFP, HMBS, HSPA8, HYLS1, HYOU1, IFT46, IL10RA, JAML, JHY, KCNJ1, KCNJ5, KIRREL3, KMT2A, LINC02873, LOC101929473, MCAM, MFRP, MIR100, MIR125B1, MIRLET7A2, MPZL2, MPZL3, MSANTD2, NECTIN1, NFRKB, NLRX1, NRGN, NXPE2, NXPE4, OAF, OR10G4, OR10G7, OR10G8, OR10G9, OR10S1, OR4D5, OR6M1, OR6T1, OR6X1, OR8A1, OR8B12, OR8B2, OR8B3, OR8B4, OR8B8, OR8D1, OR8D2, OR8D4, OR8G1, OR8G5, PAFAH1B2, PANX3, PATE1, PATE2, PATE3, PATE4, PCSK7, PDZD3, PHLDB1, PKNOX2, POU2F3, PRDM10, PUS3, RNF214, RNF26, ROBO3, ROBO4, RPS25, RPUSD4, SC5D, SCN2B, SCN3B, SCN4B, SIAE, SIDT2, SIK3, SLC37A2, SLC37A4, SNX19, SORL1, SPA17, SRPRA, ST14, ST3GAL4, STT3A, TAGLN, TBCEL, TBRG1, TECTA, THY1, TIRAP, TLCD5, TMEM218, TMEM225, TMEM25, TMEM45B, TMPRSS13, TMPRSS4, TP53AIP1, TRAPPC4, TREH, TRIM29, TTC36, UBASH3B, UBE4A, UPK2, USP2, VPS11, VSIG2, VWA5A, ZBTB44, ZNF202, ZPR1 0 1 0 0 0 0 0 1
ABITRAM, ACTL7A, CTNNAL1, ELP1, MIR32, TMEM245 0 0 1 0 0 0 0 1
ACP6, BCL9, CHD1L, FMO5, GJA5, GJA8, GPR89B, PRKAB2 1 0 0 0 0 0 0 1
ACVR2A, ARHGAP15, ARL5A, CACNB4, CXCR4, DARS1, EPC2, GTDC1, HNMT, KYNU, LCT, LRP1B, LYPD6, LYPD6B, MBD5, MCM6, MMADHC, NEB, NMI, NXPH2, ORC4, R3HDM1, RBM43, RIF1, RND3, SPOPL, THSD7B, TNFAIP6, UBXN4, ZEB2 1 0 0 0 0 0 0 1
ADAMTS8 0 0 1 0 0 0 0 1
ADGRG1 1 0 0 0 0 0 0 1
AFG3L2, TUBB6 1 0 0 0 0 0 0 1
AHCTF1 0 0 1 0 0 0 0 1
ALKBH5, ATPAF2, COPS3, DRC3, DRG2, FLCN, FLII, GID4, LLGL1, MED9, MIEF2, MIR33B, MPRIP, MYO15A, NT5M, PEMT, PLD6, RAI1, RASD1, SREBF1, TOM1L2, TOP3A 1 0 0 0 0 0 0 1
ALX4 0 0 1 0 0 0 0 1
AMH 0 0 0 1 0 0 0 1
ANKRD11 1 0 0 0 0 0 0 1
APTX 0 0 1 0 0 0 0 1
ASXL3 0 0 1 0 0 0 0 1
ATP10A, GABRA5, GABRB3, GABRG3, GOLGA8M, HERC2, IPW, MAGEL2, MKRN3, NDN, NPAP1, OCA2, PWAR1, PWAR4, PWAR5, PWAR6, PWARSN, PWRN1, PWRN2, SNORD115-1, SNORD116-1, SNRPN, SNURF, UBE3A 1 0 0 0 0 0 0 1
ATP5PO 0 1 0 0 0 0 0 1
BCDIN3D 0 0 0 1 0 0 0 1
BCORL1 0 0 1 0 0 0 0 1
BSN 0 0 1 0 0 0 0 1
CACNA1A 0 1 0 0 0 0 0 1
CLUH, METTL16, PAFAH1B1, RAP1GAP2 1 0 0 0 0 0 0 1
CNGB3 1 0 0 0 0 0 0 1
COL18A1 0 1 0 0 0 0 0 1
COL18A1, SLC19A1 0 1 0 0 0 0 0 1
COL1A2 0 0 1 0 0 0 0 1
CYRIA, DDX1, MYCN, MYCNOS 0 1 0 0 0 0 0 1
DLD, LAMB1 0 0 0 0 1 0 0 1
DMBX1 0 1 0 0 0 0 0 1
EBF3 0 1 0 0 0 0 0 1
EFEMP1 0 1 0 0 0 0 0 1
ELP4, PAX6 0 1 0 0 0 0 0 1
EME2, MRPS34 0 1 0 0 0 0 0 1
FBN2 0 0 1 0 0 0 0 1
FOXG1 1 0 0 0 0 0 0 1
FOXP1 0 1 0 0 0 0 0 1
FRMD7, GPC3, GPC4, HS6ST2, IGSF1, MBNL3, OR13H1, RAP2C, STK26, TFDP3, USP26 1 0 0 0 0 0 0 1
GFOD1, MCUR1, NOL7, PHACTR1, RANBP9, RNF182, SIRT5, TBC1D7 0 0 1 0 0 0 0 1
GYG2 0 0 0 0 0 0 1 1
HSPB7 0 0 0 1 0 0 0 1
INPP4A 0 1 0 0 0 0 0 1
INTS6L 0 0 1 0 0 0 0 1
ISCA2 0 1 0 0 0 0 0 1
KCNV2 1 0 0 0 0 0 0 1
KDM6B 0 0 1 0 0 0 0 1
KIF7 0 1 0 0 0 0 0 1
LMBR1, MNX1, NOM1 0 0 1 0 0 0 0 1
LMBR1, RNF32 0 0 1 0 0 0 0 1
LSM1 0 0 1 0 0 0 0 1
MIP 0 0 1 0 0 0 0 1
MPP4 1 0 0 0 0 0 0 1
MRPS34 1 0 0 0 0 0 0 1
MT-CO1, MT-TS1 1 0 0 0 1 0 0 1
MTFMT 1 0 0 0 0 0 0 1
MYO5A 1 0 0 0 0 0 0 1
NALCN 1 0 0 0 0 0 0 1
NDP 0 1 0 0 0 0 0 1
NDUFA2 0 0 1 0 0 0 0 1
NDUFS2 0 1 0 0 0 0 0 1
NFIX 0 1 0 0 0 0 0 1
NMNAT1 0 1 0 0 0 0 0 1
NPIPA5 0 0 1 0 0 0 0 1
NR2F1 0 0 1 0 0 0 0 1
OAT 0 1 0 0 0 0 0 1
OPHN1 0 1 0 0 0 0 0 1
OTX2 0 1 0 0 0 0 0 1
PCDH19 1 0 0 0 0 0 0 1
PIGQ 0 1 0 0 0 0 0 1
POGZ 1 0 0 0 0 0 0 1
PRICKLE3 0 0 0 0 0 1 0 1
RHO 1 0 0 0 0 0 0 1
RP1 0 0 1 0 0 0 0 1
RPE65 1 0 0 0 0 0 0 1
RSRC2 0 1 0 0 0 0 0 1
SETX 0 1 0 0 0 0 0 1
SIL1 1 0 0 0 0 0 0 1
SIX6 1 0 0 0 0 0 0 1
SLC2A1 1 0 0 0 0 0 0 1
SMARCA4 0 0 0 1 0 0 0 1
SOX3 0 0 1 0 0 0 0 1
SOX5 0 1 0 0 0 0 0 1
SPART 0 1 0 0 0 0 0 1
STXBP1 1 0 0 0 0 0 0 1
TBC1D24 0 0 1 0 0 0 0 1
TFAP2A 1 0 0 0 0 0 0 1
TIMMDC1 0 0 1 0 0 0 0 1
TMCO1 1 0 0 0 0 0 0 1
ZNF787 0 0 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 117
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign risk factor not provided total
Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine 21 13 772 327 637 0 0 1770
Illumina Clinical Services Laboratory,Illumina 8 5 1193 133 389 0 0 1728
Invitae 195 37 158 283 41 0 0 714
Counsyl 38 176 117 10 0 0 0 341
Natera, Inc. 38 2 138 30 31 0 0 239
OMIM 169 0 1 0 0 1 0 171
Integrated Genetics/Laboratory Corporation of America 101 35 2 3 15 0 0 156
GeneReviews 101 0 3 0 1 0 0 105
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories 28 14 15 17 28 0 0 102
Baylor Genetics 23 16 60 0 0 0 0 99
Centre for Mendelian Genomics,University Medical Centre Ljubljana 30 23 23 1 1 0 0 78
Fulgent Genetics,Fulgent Genetics 18 6 41 0 0 0 0 65
Mendelics 15 17 10 3 8 0 0 53
CHU Sainte-Justine Research Center,University of Montreal 1 0 6 20 0 0 0 27
Genetic Services Laboratory, University of Chicago 19 5 2 0 0 0 0 26
Institute of Human Genetics, Klinikum rechts der Isar 16 6 0 0 0 0 0 22
Genomic Research Center, Shahid Beheshti University of Medical Sciences 2 4 14 0 0 0 0 20
GenomeConnect, ClinGen 0 0 0 0 0 0 19 19
Myriad Women's Health, Inc. 5 14 0 0 0 0 0 19
Talkowski Laboratory, Center for Human Genetic Research,Massachusetts General Hospital 7 2 9 0 0 0 0 18
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 1 0 2 5 10 0 0 18
SingHealth Duke-NUS Institute of Precision Medicine 3 3 5 0 0 0 0 11
Neurogenetics,IRCCS Istituto delle Scienze Neurologiche di Bologna 11 0 0 0 0 0 0 11
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine 9 1 0 0 0 0 0 10
NIHR Bioresource Rare Diseases, University of Cambridge 6 3 0 0 0 0 0 9
SIB Swiss Institute of Bioinformatics 0 3 4 1 1 0 0 9
Biochemical Molecular Genetic Laboratory,King Abdulaziz Medical City 3 3 2 0 0 0 0 8
Broad Institute Rare Disease Group, Broad Institute 0 1 7 0 0 0 0 8
Engle Laboratory,Boston Children's Hospital 5 2 0 0 0 0 0 7
Victorian Clinical Genetics Services,Murdoch Childrens Research Institute 2 5 0 0 0 0 0 7
Laboratory of Metabolic Disorders, Peking University First Hospital 7 0 0 0 0 0 0 7
Center for Neuroscience and Cell Biology,University of Coimbra, Portugal 0 3 4 0 0 0 0 7
CHLA Center for Personalized Medicine,Children's Hospital, Los Angeles 1 3 3 0 0 0 0 7
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine 3 3 0 0 0 0 0 6
ClinVar Staff, National Center for Biotechnology Information (NCBI) 0 0 0 0 0 0 6 6
Developmental Genetics Unit,King Faisal Specialist Hospital & Research Centre 0 6 0 0 0 0 0 6
University of Washington Center for Mendelian Genomics, University of Washington 0 6 0 0 0 0 0 6
Knight Diagnostic Laboratories, Oregon Health and Sciences University 2 3 1 0 0 0 0 6
Institute of Human Genetics, University of Leipzig Medical Center 4 1 0 1 0 0 0 6
UCLA Clinical Genomics Center, UCLA 1 4 0 0 0 0 0 5
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 3 1 1 0 0 0 0 5
Institute for Genomic Medicine, Columbia University,Columbia University Medical Center 5 0 0 0 0 0 0 5
Soonchunhyang University Bucheon Hospital,Soonchunhyang University Medical Center 1 1 3 0 0 0 0 5
The Molecular Genetic and Pathologic Diagnosis Center of Neuromuscular Disorder,Children's Hospital of Fudan University 2 3 0 0 0 0 0 5
Centogene AG - the Rare Disease Company 4 0 0 0 0 0 0 4
CSER _CC_NCGL, University of Washington 1 0 3 0 0 0 0 4
Hadassah Hebrew University Medical Center 1 3 0 0 0 0 0 4
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 2 1 0 0 0 1 0 4
Geisinger Autism and Developmental Medicine Institute,Geisinger Health System 0 0 4 0 0 0 0 4
Institute of Medical Molecular Genetics, University of Zurich 0 3 0 0 0 0 0 3
Mayo Clinic Laboratories, Mayo Clinic 2 0 1 0 0 0 0 3
Center of Genomic medicine, Geneva,University Hospital of Geneva 2 1 0 0 0 0 0 3
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 1 2 0 0 0 0 0 3
Institute for Genomic Medicine, Nationwide Children's Hospital 1 2 0 0 0 0 0 3
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota 1 2 0 0 0 0 0 3
New York Genome Center 0 0 3 0 0 0 0 3
Athena Diagnostics Inc 0 0 0 0 2 0 0 2
Elsea Laboratory,Baylor College of Medicine 1 0 1 0 0 0 0 2
Institute of Human Genetics,Cologne University 0 1 1 0 0 0 0 2
Samuels research lab,Centre de Recherche du CHU Ste-Justine 2 0 0 0 0 0 0 2
Department of Mental Retardation and Birth Defect Research, National Center of Neurology and Psychiatry 0 2 0 0 0 0 0 2
Institute of Human Genetics, Uniklinik RWTH Aachen 0 0 2 0 0 0 0 2
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 0 2 0 0 0 0 0 2
Gene Discovery Core-Manton Center,Boston Children's Hospital 2 0 0 0 0 0 0 2
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 0 1 1 0 0 0 0 2
Groupe Hospitalier Pitie Salpetriere, UF Genomique du Developpement,Assistance Publique Hopitaux de Paris 0 2 0 0 0 0 0 2
Department of Pathology and Laboratory Medicine,Sinai Health System 0 0 1 0 1 0 0 2
Mitochondrial Research Group,Murdoch Children's Research Institute 1 0 1 0 0 0 0 2
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 2 0 0 0 0 2
Consultorio y Laboratorio de Neurogenética,Hospital JM Ramos Mejia 0 0 2 0 0 0 0 2
Wendy Chung Laboratory,Columbia University Medical Center 0 1 1 0 0 0 0 2
UNC Molecular Genetics Laboratory,University of North Carolina at Chapel Hill 0 2 0 0 0 0 0 2
St. Jude Clinical Genomics Lab, St. Jude Children's Research Hospital 2 0 0 0 0 0 0 2
Kids Research, The Children's Hospital at Westmead 0 2 0 0 0 0 0 2
Institute for Genomic Medicine (IGM) Clinical Laboratory,Nationwide Children's Hospital 1 0 1 0 0 0 0 2
Mitochondrial Disorders Lab i+12, Hospital Universitario 12 de Octubre 2 0 0 0 0 0 0 2
Research Unit for Rare Diseases,1st Faculty of Medicine, Charles University in Prague 2 0 0 0 0 0 0 2
Myelin Disorders Clinic-Children's Medical Center/Medical Genetics Lab-Tarbiat Modares University, Children's Medical Center, Pediatrics Center of Excellence, 1 0 1 0 0 0 0 2
Molecular Medicine for Neurodegenerative and Neuromuscular Diseases Unit,IRCCS Fondazione Stella Maris 2 0 0 0 0 0 0 2
Division of Genomic Medicine, Department of Advanced Medicine, Medical Research Institute,Kanazawa Medical University 1 1 0 0 0 0 0 2
Courtagen Diagnostics Laboratory,Courtagen Life Sciences 1 0 0 0 0 0 0 1
Shenzhen Institute of Pediatrics,Shenzhen Children's Hospital 0 0 1 0 0 0 0 1
Simons Lab, The University of Queensland 1 0 0 0 0 0 0 1
Clinical Genetics Karolinska University Hospital,Karolinska University Hospital 0 1 0 0 0 0 0 1
Mutsuddi Laboratory, Department of Molecular and Human Genetics,Banaras Hindu University 1 0 0 0 0 0 0 1
Division of Human Genetics,Children's Hospital of Philadelphia 0 1 0 0 0 0 0 1
Tgen's Center For Rare Childhood Disorders,Translational Genomics Research Institute (TGEN) 1 0 0 0 0 0 0 1
Agency for Science, Technology and Research,Genome Institute of Singapore 1 0 0 0 0 0 0 1
National Institute on Deafness and Communication Disorders,National Institutes of Health 0 0 1 0 0 0 0 1
Erez Levanon lab,Bar Ilan University 1 0 0 0 0 0 0 1
Centre for Molecular Medicine and Therapeutics,University of British Columbia 0 1 0 0 0 0 0 1
Clinics for Rare Diseases Referral (Hong Kong),The University of Hong Kong 0 1 0 0 0 0 0 1
Human Genetics - Radboudumc,Radboudumc 0 1 0 0 0 0 0 1
GenePathDx,Causeway Health Care Private Ltd 1 0 0 0 0 0 0 1
Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences 0 1 0 0 0 0 0 1
Daryl Scott Lab,Baylor College of Medicine 1 0 0 0 0 0 0 1
Undiagnosed Diseases Network,NIH 1 0 0 0 0 0 0 1
Human Molecular Genetics and Metabolic Disorders,Pakistan Institute for Engineering and Applied Science (PIEAS) 1 0 0 0 0 0 0 1
Biologia e Medicina Molecolare, Sapienza University of Rome 1 0 0 0 0 0 0 1
Genetics of Mitochondrial Diseases,Imagine Institute 0 1 0 0 0 0 0 1
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center 0 0 0 1 0 0 0 1
Gill Bejerano Lab,Stanford University 0 1 0 0 0 0 0 1
Laboratoire de Genetique Moleculaire,Centre Hospitalier Universitaire de Bordeaux 1 0 0 0 0 0 0 1
Department of Genetics,Sultan Qaboos University Hospital, Oman 1 0 0 0 0 0 0 1
HSP Biomedical Diagnostics Department,Hospital San Pedro 0 1 0 0 0 0 0 1
Unit of Genetics of Neurodegenerative and Metabolic Disease,Fondazione IRCCS Istituto Neurologico Carlo Besta 1 0 0 0 0 0 0 1
Breda Genetics srl 1 0 0 0 0 0 0 1
Clinical Genetics, Amsterdam Medical Centre 0 0 1 0 0 0 0 1
Leeds Institute of Medical Research,University of Leeds 1 0 0 0 0 0 0 1
Molecular Diagnostics, Microbiology, Virology, Parasitology and Genetics,Sofia University, St. Kliment Ohridski 0 1 0 0 0 0 0 1
Reproductive Health Research and Development,BGI Genomics 1 0 0 0 0 0 0 1
Laboratory for Population and Evolutionary Genetics,University of Puerto Rico at Mayaguez 1 0 0 0 0 0 0 1
Diagnostics Lab (ASPIRE), CSIR - Centre for Cellular and Molecular Biology 0 0 1 0 0 0 0 1
Genetics Institute, Tel Aviv Sourasky Medical Center 0 0 1 0 0 0 0 1
Cardiogenetic Research Center,Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences 1 0 0 0 0 0 0 1
Nilou-Genome Lab 0 0 1 0 0 0 0 1
Medical Genetics Laboratory,CHRU Nancy 1 0 0 0 0 0 0 1

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