ClinVar Miner

Variants studied for hereditary generalized epilepsy

Included ClinVar conditions (61):
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 association risk factor not provided total
430 215 4396 3670 1030 1 19 47 9364

Gene and significance breakdown #

Total genes and gene combinations: 67
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign association risk factor not provided total
CACNA1H 1 1 1137 1495 699 0 4 6 3043
SCN1A, SCN9A 75 23 1132 621 69 0 0 5 1903
GABRG2 75 32 252 169 26 0 0 0 529
GABRA1 27 17 242 174 42 0 4 0 484
GABRB3 37 20 191 199 22 0 3 1 466
SCN9A 17 7 232 129 7 0 0 1 392
EFHC1 2 0 243 107 33 1 5 1 363
RBFOX1 0 0 174 165 16 0 0 0 355
GABRD 0 0 146 165 20 0 0 0 331
STX1B 27 24 111 121 18 0 0 0 297
RBFOX3 0 0 113 148 13 0 0 0 272
LOC102724058, SCN1A 57 27 94 13 9 0 0 16 205
CACNB4 1 1 97 70 19 0 1 2 186
SCN1A 70 34 62 7 5 0 1 11 185
SCN1B 3 3 48 15 11 0 0 1 80
CLCN2 2 8 20 20 3 0 1 0 52
LOC126862278, RBFOX1 0 0 20 18 3 0 0 0 41
LOC126862279, RBFOX1 0 0 19 16 3 0 0 0 38
HCN1 8 5 20 3 0 0 0 1 36
GABRA6 0 0 3 7 11 0 0 0 21
CACNB4, LOC129934925 0 0 8 8 1 0 0 0 14
SLC32A1 4 4 5 0 0 0 0 0 9
ADGRV1 1 5 0 0 0 0 0 0 6
GABRB3, LOC126862078 2 0 2 0 0 0 0 0 4
CSRNP3, GALNT3, LOC100506124, LOC102724058, LOC120977013, LOC126806396, LOC129388938, LOC129935043, LOC129935044, LOC129935045, LOC129935046, LOC129935047, SCN1A, SCN2A, SCN3A, SCN9A, TTC21B 3 0 0 0 0 0 0 0 3
CSRNP3, GALNT3, SCN1A, SCN2A, SCN3A, SCN9A, TTC21B 2 0 1 0 0 0 0 0 3
CACNA1G 0 0 0 0 0 0 0 2 2
GABRA1, GABRA6, GABRB2, GABRG2 1 0 1 0 0 0 0 0 2
GABRA1, GABRG2 1 1 0 0 0 0 0 0 2
HSD3B7, STX1B 1 0 1 0 0 0 0 0 2
LOC130058887, STX1B 2 0 0 0 0 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 0 0 1
ABCA3, AMDHD2, ANTKMT, ATP6V0C, AXIN1, BAIAP3, BICDL2, BRICD5, C16orf90, C1QTNF8, CACNA1H, CAPN15, CASKIN1, CCDC154, CCDC78, CCNF, CEMP1, CHTF18, CIAO3, CLCN7, CLDN6, CLDN9, CLUAP1, CRAMP1, DECR2, DNASE1, DNASE1L2, E4F1, ECI1, ELOB, EME2, FAHD1, FBXL16, FLYWCH1, FLYWCH2, GFER, GNG13, GNPTG, HAGH, HAGHL, HCFC1R1, HS3ST6, IFT140, IGFALS, IL32, JMJD8, JPT2, KCTD5, KREMEN2, LMF1, MAPK8IP3, MCRIP2, MEFV, MEIOB, METRN, METTL26, MIR1225, MLST8, MMP25, MRPL28, MRPS34, MSLN, MSRB1, MTRNR2L4, NAA60, NDUFB10, NHERF2, NHLRC4, NLRC3, NME3, NME4, NOXO1, NPW, NTHL1, NTN3, NUBP2, OR1F1, OR2C1, PAQR4, PDPK1, PGAP6, PGP, PIGQ, PKD1, PKMYT1, PRR25, PRR35, PRSS21, PRSS22, PRSS27, PRSS33, PRSS41, PTX4, RAB11FIP3, RAB26, RAB40C, RHBDL1, RHOT2, RNF151, RNPS1, RPL3L, RPS2, RPUSD1, SLX4, SNHG9, SOX8, SPSB3, SRRM2, SSTR5, STUB1, SYNGR3, TBC1D24, TBL3, TEDC2, TELO2, THOC6, TIGD7, TMEM204, TNFRSF12A, TPSAB1, TPSB2, TPSD1, TPSG1, TRAF7, TRAP1, TSC2, TSR3, UBE2I, UNKL, UQCC4, WDR24, WDR90, WFIKKN1, ZG16B, ZNF174, ZNF200, ZNF205, ZNF213, ZNF263, ZNF597, ZNF598, ZNF75A, ZSCAN10, ZSCAN32 0 0 1 0 0 0 0 0 1
ABCA3, ANTKMT, BAIAP3, BRICD5, C1QTNF8, CACNA1H, CASKIN1, CCDC154, CCDC78, CCNF, CHTF18, CIAO3, CLCN7, CRAMP1, DNASE1L2, E4F1, ECI1, EME2, FAHD1, FBXL16, GFER, GNG13, GNPTG, HAGH, HAGHL, HS3ST6, IFT140, IGFALS, JMJD8, JPT2, LMF1, MAPK8IP3, MCRIP2, MEIOB, METRN, METTL26, MIR1225, MLST8, MRPS34, MSLN, MSRB1, NDUFB10, NHERF2, NME3, NOXO1, NPW, NTHL1, NTN3, NUBP2, PGP, PIGQ, PKD1, PRR25, PTX4, RAB26, RAB40C, RHBDL1, RHOT2, RNF151, RNPS1, RPL3L, RPS2, RPUSD1, SNHG9, SOX8, SPSB3, SSTR5, STUB1, SYNGR3, TBC1D24, TBL3, TEDC2, TELO2, TMEM204, TPSAB1, TPSB2, TPSD1, TPSG1, TRAF7, TSC2, TSR3, UBE2I, UNKL, UQCC4, WDR24, WDR90, WFIKKN1, ZNF598 0 0 1 0 0 0 0 0 1
ABCB1 0 1 0 0 0 0 0 0 1
AFMID, BIRC5, C17orf99, C1QTNF1, CANT1, CARD14, CBX2, CBX4, CBX8, CCDC40, CYTH1, DNAH17, EIF4A3, ENGASE, ENPP7, GAA, LGALS3BP, PGS1, RBFOX3, RNF213, SGSH, SLC26A11, SOCS3, SYNGR2, TBC1D16, TIMP2, TK1, TMC6, TMC8, TMEM235, USP36 0 0 1 0 0 0 0 0 1
ALKBH6, APLP1, ARHGAP33, ATP4A, CAPNS1, CD22, CLIP3, COX6B1, COX7A1, DMKN, ETV2, FAM187B, FFAR1, FFAR2, FFAR3, FXYD1, FXYD3, FXYD5, FXYD7, GAPDHS, GPR42, GRAMD1A, HAMP, HAUS5, HCST, HPN, HSPB6, IGFLR1, KIRREL2, KMT2B, KRTDAP, LGI4, LIN37, LRFN3, LSR, MAG, NFKBID, NPHS1, OVOL3, POLR2I, PRODH2, PROSER3, PSENEN, RBM42, SBSN, SCN1B, SDHAF1, SYNE4, TBCB, THAP8, TMEM147, TYROBP, U2AF1L4, UPK1A, USF2, WDR62, ZBTB32, ZFP14, ZFP82, ZNF146, ZNF181, ZNF260, ZNF30, ZNF302, ZNF345, ZNF382, ZNF383, ZNF420, ZNF461, ZNF529, ZNF565, ZNF566, ZNF567, ZNF568, ZNF585A, ZNF585B, ZNF599, ZNF790, ZNF792, ZNF829, ZNF850 1 0 0 0 0 0 0 0 1
ANKRD65, ATAD3A, ATAD3B, ATAD3C, AURKAIP1, CALML6, CCNL2, CDK11A, CDK11B, CFAP74, CPTP, DVL1, FNDC10, GABRD, GNB1, INTS11, MIB2, MMP23B, MRPL20, MXRA8, NADK, SLC35E2A, SLC35E2B, SSU72, TAS1R3, TMEM240, TMEM52, TMEM88B, VWA1 0 0 1 0 0 0 0 0 1
ANO4 1 0 0 0 0 0 0 0 1
ANTKMT, ARHGDIG, AXIN1, BAIAP3, C1QTNF8, CACNA1H, CAPN15, CCDC154, CCDC78, CHTF18, CIAO3, CLCN7, CRAMP1, DECR2, EME2, FAM234A, FBXL16, GNG13, GNPTG, HAGHL, IFT140, IGFALS, JMJD8, JPT2, LMF1, LUC7L, MAPK8IP3, MCRIP2, METRN, METTL26, MRPL28, MRPS34, MSLN, NHLRC4, NME3, NME4, NUBP2, PDIA2, PGAP6, PIGQ, PRR25, PRR35, PTX4, RAB11FIP3, RAB40C, RGS11, RHBDL1, RHOT2, RPUSD1, SOX8, SPSB3, SSTR5, STUB1, TELO2, TMEM204, TPSAB1, TPSB2, TPSD1, TPSG1, TSR3, UBE2I, UNKL, UQCC4, WDR24, WDR90, WFIKKN1 0 0 1 0 0 0 0 0 1
ANTKMT, AXIN1, C1QTNF8, CACNA1H, CAPN15, CCDC78, CHTF18, CIAO3, DECR2, FBXL16, GNG13, HAGHL, JMJD8, LMF1, MCRIP2, METRN, METTL26, MRPL28, MSLN, NHLRC4, NME4, PGAP6, PIGQ, PRR25, PRR35, RAB11FIP3, RAB40C, RHBDL1, RHOT2, RPUSD1, SOX8, SSTR5, STUB1, WDR24, WDR90, WFIKKN1 0 0 1 0 0 0 0 0 1
ANTKMT, BAIAP3, C1QTNF8, CACNA1H, CCDC154, CCDC78, CHTF18, CIAO3, CLCN7, CRAMP1, EME2, FAHD1, FBXL16, GFER, GNG13, GNPTG, HAGH, HAGHL, HS3ST6, IFT140, IGFALS, JMJD8, JPT2, LMF1, MAPK8IP3, MCRIP2, MEIOB, METRN, METTL26, MIR1225, MRPS34, MSLN, MSRB1, NDUFB10, NHERF2, NME3, NOXO1, NPW, NTHL1, NUBP2, PIGQ, PKD1, PRR25, PTX4, RAB40C, RHBDL1, RHOT2, RNF151, RPL3L, RPS2, RPUSD1, SNHG9, SOX8, SPSB3, SSTR5, STUB1, SYNGR3, TBL3, TELO2, TMEM204, TPSAB1, TPSB2, TPSD1, TPSG1, TSC2, TSR3, UBE2I, UNKL, UQCC4, WDR24, WDR90, WFIKKN1, ZNF598 0 0 1 0 0 0 0 0 1
ANTKMT, C1QTNF8, CACNA1H, CCDC78, CHTF18, CIAO3, GNG13, HAGHL, LMF1, METRN, MSLN, PRR25, RPUSD1, SOX8, SSTR5 0 0 1 0 0 0 0 0 1
ARL5A, CACNB4, NEB 0 0 1 0 0 0 0 0 1
ATP10A, GABRA5, GABRB3 1 0 0 0 0 0 0 0 1
ATP10A, GABRA5, GABRB3, GABRG3, OCA2 1 0 0 0 0 0 0 0 1
BCL7C, CFAP119, CTF1, FBXL19, HSD3B7, ORAI3, PHKG2, RNF40, SETD1A, SRCAP, STX1B, ZNF629 0 0 1 0 0 0 0 0 1
CALML6, CFAP74, FAAP20, GABRD, GNB1, MORN1, PEX10, PRKCZ, RER1, SKI, TMEM52 0 0 1 0 0 0 0 0 1
CAPRIN1 1 0 0 0 0 0 0 0 1
CASR 0 0 1 0 0 0 0 0 1
CHRNA1 0 0 1 0 0 0 0 0 1
CHRNA7 1 0 0 0 0 0 0 0 1
CSRNP3, GALNT3, LOC100506124, LOC102724058, LOC126806396, LOC129388938, LOC129935044, LOC129935045, LOC129935046, LOC129935047, SCN1A, SCN2A, SCN9A, TTC21B 0 0 1 0 0 0 0 0 1
CSRNP3, GALNT3, SCN1A, SCN2A, SCN9A, TTC21B 0 0 1 0 0 0 0 0 1
GABRA1, GABRA6 0 0 1 0 0 0 0 0 1
GABRA1, GABRA6, GABRG2 1 0 0 0 0 0 0 0 1
GABRA5, GABRB3, GABRG3, HERC2, OCA2 0 0 1 0 0 0 0 0 1
GABRB3, LOC126862077, LOC126862078 0 0 1 0 0 0 0 0 1
HCN1, LOC126807381, LOC126807382 0 0 1 0 0 0 0 0 1
HSD17B3, SLC35D2-HSD17B3 1 0 0 0 0 0 0 0 1
KCNIP1 1 0 0 0 0 0 0 0 1
LOC101927358, MIR6130, RORB 0 1 0 0 0 0 0 0 1
LOC130058885, LOC130058886, LOC130058887, STX1B, STX4, ZNF668 1 0 0 0 0 0 0 0 1
RELN, SLC26A5 0 0 1 0 0 0 0 0 1
SCN2A 1 0 0 0 0 0 0 0 1
SCN3A 0 0 1 0 0 0 0 0 1
SNAP25 0 1 0 0 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 98
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign association risk factor not provided total
Labcorp Genetics (formerly Invitae), Labcorp 253 98 3602 3442 968 0 0 0 8363
Fulgent Genetics, Fulgent Genetics 15 7 413 280 19 0 0 0 734
Illumina Laboratory Services, Illumina 1 0 337 119 57 0 0 0 513
OMIM 35 0 8 0 0 0 19 0 62
Baylor Genetics 7 6 49 0 0 0 0 0 62
Mendelics 41 8 2 0 2 0 0 0 53
Institute of Human Genetics, University of Leipzig Medical Center 13 14 24 1 1 0 0 0 53
New York Genome Center 0 1 44 0 0 0 0 0 45
Juno Genomics, Hangzhou Juno Genomics, Inc 4 8 13 0 0 0 0 0 25
UniProtKB/Swiss-Prot 0 0 0 0 0 0 0 24 24
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 5 1 14 4 0 0 0 0 24
Neuberg Centre For Genomic Medicine, NCGM 4 2 17 0 0 0 0 0 23
Génétique des Maladies du Développement, Hospices Civils de Lyon 12 6 3 0 0 0 0 0 21
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 6 1 8 0 0 0 0 0 15
Lifecell International Pvt. Ltd 6 4 5 0 0 0 0 0 15
Athena Diagnostics 0 0 0 0 12 0 0 0 12
MGZ Medical Genetics Center 0 5 7 0 0 0 0 0 12
3billion 4 2 4 1 0 0 0 0 11
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 9 1 0 0 0 0 0 0 10
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 0 0 10 10
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München 6 3 0 0 0 0 0 0 9
Neurogenetics Research Program, University of Adelaide 0 4 4 0 0 0 0 0 8
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 0 0 8 0 0 0 8
Department of Neurology, Hunan Children's Hospital 3 1 4 0 0 0 0 0 8
Genomic Research Center, Shahid Beheshti University of Medical Sciences 1 1 4 1 0 0 0 0 7
Paris Brain Institute, Inserm - ICM 2 5 0 0 0 0 0 0 7
GenomeConnect - Brain Gene Registry 0 0 0 0 0 0 0 7 7
Genetic Services Laboratory, University of Chicago 4 2 0 0 0 0 0 0 6
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 0 0 6 0 0 0 0 0 6
GenomeConnect, ClinGen 0 0 0 0 0 0 0 6 6
Genome-Nilou Lab 2 0 0 0 4 0 0 0 6
Genome Diagnostics Laboratory, University Medical Center Utrecht 0 0 0 0 5 0 0 0 5
Mayo Clinic Laboratories, Mayo Clinic 0 0 5 0 0 0 0 0 5
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 1 2 2 0 0 0 0 0 5
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille 3 2 0 0 0 0 0 0 5
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues 0 2 3 0 0 0 0 0 5
Diagnostic Genetics, Severance Hospital, Yonsei University College of Medicine 0 5 0 0 0 0 0 0 5
Uskudar University, Department of Molecular Biology and Genetics, Uskudar University 5 0 0 0 0 0 0 0 5
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 2 0 0 0 2 0 0 0 4
Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn 1 1 2 0 0 0 0 0 4
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein 1 1 2 0 0 0 0 0 4
School Of Forensic, Xinxiang Medical University 0 4 0 0 0 0 0 0 4
Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin 1 0 2 0 0 0 0 0 3
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 1 2 0 0 0 0 0 0 3
Cavalleri Lab, Royal College of Surgeons in Ireland 1 2 0 0 0 0 0 0 3
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology 2 0 1 0 0 0 0 0 3
Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center 0 0 3 0 0 0 0 0 3
Cell and Molecular Biology Laboratory, University of the Punjab Lahore 0 1 1 0 0 1 0 0 3
DASA 2 1 0 0 0 0 0 0 3
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 2 1 0 0 0 0 0 3
Institute of Immunology and Genetics Kaiserslautern 2 1 0 0 0 0 0 0 3
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital 0 0 2 0 0 0 0 0 2
Revvity Omics, Revvity 0 0 2 0 0 0 0 0 2
Institute for Genomic Medicine (IGM) Clinical Laboratory, Nationwide Children's Hospital 2 0 0 0 0 0 0 0 2
Centogene AG - the Rare Disease Company 0 0 2 0 0 0 0 0 2
Centre for Inherited Metabolic Diseases, Karolinska University Hospital 0 0 2 0 0 0 0 0 2
Soonchunhyang University Bucheon Hospital, Soonchunhyang University Medical Center 0 0 1 0 1 0 0 0 2
Center for Statistical Genetics, Columbia University 1 1 0 0 0 0 0 0 2
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India 2 0 0 0 0 0 0 0 2
Experimental Epileptology, AG Lerche, Hertie Institute for Clinical Brain Research 0 0 1 0 1 0 0 0 2
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City 0 0 2 0 0 0 0 0 2
Breda Genetics srl 0 0 2 0 0 0 0 0 2
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas 0 0 2 0 0 0 0 0 2
Molecular Genetics Lab, CHRU Brest 2 0 0 0 0 0 0 0 2
Palindrome, Gene Kavoshgaran Aria 2 0 0 0 0 0 0 0 2
Solve-RD Consortium 0 2 0 0 0 0 0 0 2
Institute of Human Genetics, University of Goettingen 0 0 1 0 0 0 0 0 1
Ambry Genetics 0 1 0 0 0 0 0 0 1
Institute of Human Genetics, Cologne University 0 1 0 0 0 0 0 0 1
Clinical Genomics Laboratory, Washington University in St. Louis 0 0 1 0 0 0 0 0 1
Institute for Human Genetics and Genomic Medicine, Uniklinik RWTH Aachen 0 0 1 0 0 0 0 0 1
Division of Human Genetics, Children's Hospital of Philadelphia 0 1 0 0 0 0 0 0 1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 1 0 0 0 0 0 0 0 1
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 0 1 0 0 0 0 0 1
NeuroMeGen, Hospital Clinico Santiago de Compostela 0 1 0 0 0 0 0 0 1
Neurogenetics group, VIB, Antwerp, Belgium 0 1 0 0 0 0 0 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 0 1 0 0 0 0 0 1
Undiagnosed Diseases Network, NIH 1 0 0 0 0 0 0 0 1
Phosphorus, Inc. 0 0 1 0 0 0 0 0 1
Institute of Medical Genetics, University of Zurich 1 0 0 0 0 0 0 0 1
Geisinger Autism and Developmental Medicine Institute, Geisinger Health System 0 0 1 0 0 0 0 0 1
New Leaf Center 0 0 0 0 1 0 0 0 1
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 0 0 1 0 0 0 0 0 1
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota 0 1 0 0 0 0 0 0 1
Genomic Medicine Lab, University of California San Francisco 0 0 1 0 0 0 0 0 1
Institute of Human Genetics, University Hospital Muenster 0 0 1 0 0 0 0 0 1
Epilepsy and Neurogenetic Laboratory, Kaohsiung Chang Gung Memorial Hospital 0 1 0 0 0 0 0 0 1
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ 0 0 1 0 0 0 0 0 1
Pediatrics, MediClubGeorgia 0 1 0 0 0 0 0 0 1
Suma Genomics 1 0 0 0 0 0 0 0 1
Molecular Genetics, Royal Melbourne Hospital 0 0 1 0 0 0 0 0 1
Neurology Department, Shenzhen Children's Hospital 1 0 0 0 0 0 0 0 1
School of Medicine NGS Core Facility, Fu Jen Catholic University 0 0 1 0 0 0 0 0 1
Department of Human Genetics, Hannover Medical School 0 1 0 0 0 0 0 0 1
Clinical Laboratory Sciences Program (CLSP), King Saud bin Abdulaziz University for Health Sciences (KSAU-HS) 1 0 0 0 0 0 0 0 1
Payam Genetics Center, General Welfare Department of North Khorasan Province 1 0 0 0 0 0 0 0 1
Department of Clinical Genetics, Medical University of Lodz 1 0 0 0 0 0 0 0 1
Regional Center For Medical Genetics Timis, Louis Turcanu Emergency Hospital for Children Timisoara 0 0 1 0 0 0 0 0 1

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