ClinVar Miner

Variants studied for familial partial epilepsy

Included ClinVar conditions (36):
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 pathogenic, low penetrance not provided total
755 364 5870 5569 782 1 121 12981

Gene and significance breakdown #

Total genes and gene combinations: 98
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign pathogenic, low penetrance not provided total
RELN 41 17 1013 1040 152 0 7 2208
DEPDC5 250 92 876 633 62 0 66 1908
KCNT1 34 18 740 991 120 0 5 1849
GRIN2A 137 138 660 718 169 0 10 1712
KCNMA1 12 11 492 510 38 0 4 1023
CHRNA4 3 2 314 356 48 0 4 702
HBA-LCR, NPRL3 75 34 317 220 29 0 2 665
CHRNA2 2 1 336 260 65 0 3 640
RELN, SLC26A5 7 1 225 235 25 0 1 474
CHRNB2 4 3 244 201 18 0 3 463
LGI1 37 15 196 137 10 0 6 391
NPRL3 36 6 81 19 1 0 0 143
PRIMA1 4 0 63 64 6 0 0 137
LOC126860130, RELN, SLC26A5 2 1 37 50 7 0 1 95
CHRNA4, LOC126863087 0 0 24 38 4 0 2 64
CHRNA4, LOC100130587 0 0 25 33 6 0 0 60
SCN3A 7 2 37 4 9 0 1 58
GAL 1 0 35 13 5 0 0 54
LOC126860131, RELN 0 0 17 33 5 0 0 54
CPA6 3 0 37 1 2 0 0 42
NPRL2 6 9 23 0 0 0 1 36
ARFGEF1-DT, CPA6 1 0 29 5 1 0 0 35
CHRNB2, LOC129931511 0 0 13 6 0 0 0 19
SZT2 11 0 0 0 0 0 0 11
SPTAN1 7 0 1 0 0 0 0 8
CHRNA4, KCNQ2 0 0 7 0 0 0 0 7
MICAL1 1 2 2 2 0 0 0 7
CNTNAP2 6 0 0 0 0 0 0 6
GABRG2 3 3 0 0 0 0 0 6
SCN1A, SCN9A 5 0 0 0 0 0 0 5
CHD2 4 0 0 0 0 0 0 4
KCNQ3 4 0 0 0 0 0 0 4
MPG, NPRL3, POLR3K, RHBDF1, SNRNP25 3 0 1 0 0 0 0 4
NPR2, SPAG8 0 3 1 0 0 0 0 4
ASAH1 3 0 0 0 0 0 0 3
DEPDC5, PRR14L 2 1 0 0 0 0 0 3
PRICKLE1 3 0 0 0 0 0 0 3
RBFOX1 3 0 0 0 0 0 0 3
SPAG1 3 0 0 0 0 0 0 3
STRADA 3 0 0 0 0 0 0 3
ABAT, CARHSP1, GRIN2A, HAPSTR1, PMM2, TMEM186, USP7 1 0 1 0 0 0 0 2
ABHD16B, ARFRP1, CHRNA4, DNAJC5, EEF1A2, FNDC11, GMEB2, HELZ2, KCNQ2, LIME1, PPDPF, PTK6, RTEL1, SLC2A4RG, SRMS, STMN3, TNFRSF6B, TPD52L2, ZBTB46, ZGPAT 0 0 2 0 0 0 0 2
CHRNA4, EEF1A2, KCNQ2, PPDPF 0 0 2 0 0 0 0 2
CRH 0 0 0 0 0 0 2 2
DNAJC2, PMPCB, PSMC2, RELN, SLC26A5 1 0 1 0 0 0 0 2
KCNQ2 0 0 0 0 0 0 2 2
SCARB2 2 0 0 0 0 0 0 2
SCN2A 2 0 0 0 0 0 0 2
WWOX 2 0 0 0 0 0 0 2
ABAT, ATF7IP2, CARHSP1, CIITA, CLEC16A, DEXI, EMP2, GRIN2A, HAPSTR1, LITAF, NUBP1, PMM2, PRM1, PRM2, PRM3, RMI2, SOCS1, TEKT5, TMEM186, TNP2, TVP23A, USP7 0 0 1 0 0 0 0 1
ABCA2, ABO, ADAMTS13, ADAMTSL2, AGPAT2, AJM1, AK8, BARHL1, BRD3, C8G, C9orf163, CACFD1, CAMSAP1, CARD9, CCDC183, CEL, CFAP77, CLIC3, COL5A1, DBH, DDX31, DIPK1B, DNLZ, DPP7, EDF1, EGFL7, ENTPD2, ENTR1, FAM163B, FBXW5, FCN1, FCN2, FUT7, GBGT1, GFI1B, GLT6D1, GPSM1, GRIN1, GTF3C4, GTF3C5, INPP5E, KCNT1, LCN1, LCN10, LCN12, LCN15, LCN6, LCN8, LCN9, LCNL1, LHX3, LINC02907, LINC02908, MAMDC4, MAN1B1, MED22, MIR126, MRPS2, MYMK, NACC2, NOTCH1, NPDC1, OBP2A, OBP2B, OLFM1, PAEP, PAXX, PHPT1, PIERCE1, PMPCA, PPP1R26, PTGDS, QSOX2, RABL6, RALGDS, REXO4, RNU6ATAC, RPL7A, RXRA, SAPCD2, SARDH, SEC16A, SETX, SLC2A6, SNAPC4, SNHG7, SOHLH1, SPACA9, STKLD1, SURF1, SURF2, SURF4, SURF6, TMEM141, TMEM250, TRAF2, TSC1, TTF1, UAP1L1, UBAC1, VAV2, WDR5 0 0 1 0 0 0 0 1
ABCA2, AGPAT2, AJM1, ANAPC2, ARRDC1, C8G, C9orf163, CACNA1B, CAMSAP1, CARD9, CCDC183, CIMIP2A, CLIC3, CYSRT1, DIPK1B, DNLZ, DPH7, DPP7, EDF1, EGFL7, EHMT1, ENTPD2, ENTPD8, ENTR1, EXD3, FBXW5, FUT7, GLT6D1, GPSM1, GRIN1, INPP5E, KCNT1, LCN1, LCN10, LCN12, LCN15, LCN6, LCN8, LCN9, LCNL1, LHX3, LINC02908, LOC651337, LRRC26, MAMDC4, MAN1B1, MIR126, MRPL41, MRPS2, NACC2, NDOR1, NELFB, NOTCH1, NOXA1, NPDC1, NRARP, NSMF, OBP2A, PAEP, PAXX, PHPT1, PMPCA, PNPLA7, PTGDS, QSOX2, RABL6, RNF208, RNF224, SAPCD2, SEC16A, SLC34A3, SNAPC4, SNHG7, SOHLH1, SSNA1, STPG3, TMEM141, TMEM203, TMEM210, TMEM250, TOR4A, TPRN, TRAF2, TUBB4B, UAP1L1, UBAC1, ZMYND19 0 0 1 0 0 0 0 1
ABCA2, AGPAT2, AJM1, ANAPC2, ARRDC1, C8G, C9orf163, CAMSAP1, CARD9, CCDC183, CIMIP2A, CLIC3, CYSRT1, DIPK1B, DNLZ, DPH7, DPP7, EDF1, EGFL7, EHMT1, ENTPD2, ENTPD8, ENTR1, EXD3, FBXW5, FUT7, GPSM1, GRIN1, INPP5E, KCNT1, LCN10, LCN12, LCN15, LCN6, LCN8, LCNL1, LHX3, LINC02908, LOC651337, LRRC26, MAMDC4, MAN1B1, MIR126, MRPL41, NACC2, NDOR1, NELFB, NOTCH1, NOXA1, NPDC1, NRARP, NSMF, PAXX, PHPT1, PMPCA, PNPLA7, PTGDS, QSOX2, RABL6, RNF208, RNF224, SAPCD2, SEC16A, SLC34A3, SNAPC4, SNHG7, SSNA1, STPG3, TMEM141, TMEM203, TMEM210, TMEM250, TOR4A, TPRN, TRAF2, TUBB4B, UAP1L1, UBAC1, ZMYND19 0 0 1 0 0 0 0 1
ABCA2, AGPAT2, AJM1, C8G, C9orf163, CAMSAP1, CARD9, CCDC183, CLIC3, DIPK1B, DNLZ, DPP7, EDF1, EGFL7, ENTPD2, ENTR1, FBXW5, FUT7, GPSM1, GRIN1, INPP5E, KCNT1, LCN10, LCN12, LCN15, LCN6, LCN8, LCNL1, LHX3, LINC02908, MAMDC4, MAN1B1, MIR126, NACC2, NOTCH1, NPDC1, PAXX, PHPT1, PMPCA, PTGDS, QSOX2, RABL6, SAPCD2, SEC16A, SNAPC4, SNHG7, TMEM141, TMEM250, TRAF2, UAP1L1, UBAC1 0 0 1 0 0 0 0 1
ABHD16B, ARFRP1, CHRNA4, DNAJC5, EEF1A2, FNDC11, GMEB2, HELZ2, KCNQ2, LIME1, PPDPF, PRPF6, PTK6, RTEL1, SAMD10, SLC2A4RG, SOX18, SRMS, STMN3, TNFRSF6B, TPD52L2, UCKL1, ZBTB46, ZGPAT, ZNF512B 0 0 1 0 0 0 0 1
ADAR, CHRNB2 0 0 1 0 0 0 0 1
ANO4 0 1 0 0 0 0 0 1
APP 0 0 1 0 0 0 0 1
ARFGAP1, BHLHE23, BIRC7, CHRNA4, COL20A1, COL9A3, DIDO1, EEF1A2, GID8, HAR1A, HAR1B, KCNQ2, NKAIN4, SLC17A9, TCFL5, YTHDF1 0 0 1 0 0 0 0 1
C9orf163, CAMSAP1, CARD9, DNLZ, ENTR1, GPSM1, INPP5E, KCNT1, LHX3, NACC2, NOTCH1, PMPCA, QSOX2, SEC16A, SNAPC4, TMEM250, UBAC1 0 0 1 0 0 0 0 1
CCDC25, CHRNA2, CLU, ELP3, EPHX2, ESCO2, EXTL3, FBXO16, FZD3, NUGGC, PBK, PNOC, SCARA3, SCARA5, ZNF395 0 0 1 0 0 0 0 1
CEP55, FFAR4, FRA10AC1, LGI1, MYOF, PDE6C, RBP4 1 0 0 0 0 0 0 1
CLCN2 0 0 1 0 0 0 0 1
CLCNKB, LOC106501713 1 0 0 0 0 0 0 1
CRH, LOC130000523 0 0 0 0 0 0 1 1
CSTB 1 0 0 0 0 0 0 1
DEPDC5, LINC02558, LOC125446219, LOC126863124, LOC129391278, LOC130067263, LOC130067264, LOC130067265, LOC130067266, NOA3, YWHAH 0 0 0 0 0 1 0 1
DEPDC5, LOC125446219 0 0 1 0 0 0 0 1
DEPDC5, LOC125446219, LOC126863124, LOC130067262 1 0 0 0 0 0 0 1
DEPDC5, LOC130067262 1 0 0 0 0 0 0 1
DEPDC5, RFPL2 0 1 0 0 0 0 0 1
DLG5, KCNMA1 0 0 1 0 0 0 0 1
EPM2A 1 0 0 0 0 0 0 1
GRIN1 1 0 0 0 0 0 0 1
GRIN2A, LOC130058418 0 1 0 0 0 0 0 1
GRIN2B 0 0 1 0 0 0 0 1
IER3IP1 1 0 0 0 0 0 0 1
ITSN2 0 0 1 0 0 0 0 1
KAT6B 1 0 0 0 0 0 0 1
KCNA1 0 1 0 0 0 0 0 1
KCNT1, SOHLH1 0 0 1 0 0 0 0 1
LOC102724058, SCN1A 1 0 0 0 0 0 0 1
LOC102724428 1 0 0 0 0 0 0 1
LOC126805704, SNIP1 1 0 0 0 0 0 0 1
LOC126862279, RBFOX1 1 0 0 0 0 0 0 1
MAF, WWOX 1 0 0 0 0 0 0 1
MPG, NPRL3 1 0 0 0 0 0 0 1
NPR2 0 1 0 0 0 0 0 1
OPLAH 0 0 1 0 0 0 0 1
PCDH19 1 0 0 0 0 0 0 1
PLCB1 1 0 0 0 0 0 0 1
PRICKLE2 1 0 0 0 0 0 0 1
RBFOX3 1 0 0 0 0 0 0 1
SCN1A 1 0 0 0 0 0 0 1
SCN1B 1 0 0 0 0 0 0 1
SLC2A1 1 0 0 0 0 0 0 1
SLC6A1 1 0 0 0 0 0 0 1
TBC1D24 1 0 0 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 pathogenic, low penetrance not provided total
Labcorp Genetics (formerly Invitae), Labcorp 546 146 5111 5452 590 0 0 11845
Illumina Laboratory Services, Illumina 1 0 369 48 190 0 0 608
Genome-Nilou Lab 0 0 64 172 102 0 0 338
Fulgent Genetics, Fulgent Genetics 3 1 132 52 5 0 0 193
Institute of Human Genetics, University of Leipzig Medical Center 19 109 41 3 0 0 0 172
Bioinformatics Core, Luxembourg Center for Systems Biomedicine 111 0 0 0 0 0 0 111
GeneReviews 1 0 0 0 0 0 97 98
OMIM 77 0 0 0 0 0 0 77
New York Genome Center 0 5 70 0 0 0 0 75
Baylor Genetics 7 4 63 0 0 0 0 74
Revvity Omics, Revvity 2 2 64 0 0 0 0 68
Neuberg Centre For Genomic Medicine, NCGM 3 5 42 0 0 0 0 50
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 4 34 0 1 0 0 39
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 2 0 31 4 0 0 0 37
Génétique des Maladies du Développement, Hospices Civils de Lyon 21 7 7 0 0 0 0 35
Mendelics 5 8 5 9 2 0 0 29
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 13 0 13 1 0 0 0 27
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 0 3 17 1 0 0 0 21
Juno Genomics, Hangzhou Juno Genomics, Inc 5 2 10 0 0 0 0 17
GenomeConnect - Brain Gene Registry 0 0 0 0 0 0 14 14
3billion 4 1 4 3 0 0 0 12
MGZ Medical Genetics Center 0 5 5 0 0 0 0 10
Centogene AG - the Rare Disease Company 0 2 8 0 0 0 0 10
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 6 4 0 0 0 0 0 10
Genome Diagnostics Laboratory, University Medical Center Utrecht 0 0 0 7 2 0 0 9
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues 1 4 4 0 0 0 0 9
Genomic Research Center, Shahid Beheshti University of Medical Sciences 1 0 7 0 0 0 0 8
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 0 5 3 0 0 8
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City 0 5 3 0 0 0 0 8
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München 2 5 0 0 0 0 0 7
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas 0 0 7 0 0 0 0 7
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 0 1 3 2 0 0 6
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 0 6 6
Mayo Clinic Laboratories, Mayo Clinic 0 0 5 0 0 0 0 5
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 1 0 4 0 0 0 0 5
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 3 2 0 0 0 0 0 5
Genetics and Molecular Pathology, SA Pathology 2 0 3 0 0 0 0 5
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center 0 0 0 5 0 0 0 5
Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn 0 3 2 0 0 0 0 5
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital 1 1 2 0 0 0 0 4
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 0 3 1 0 0 0 0 4
Center of Genomic medicine, Geneva, University Hospital of Geneva 1 0 3 0 0 0 0 4
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 2 2 0 0 0 0 0 4
GenomeConnect, ClinGen 0 0 0 0 0 0 4 4
Laboratory of Functional Genomics, Research Centre for Medical Genetics 2 2 0 0 0 0 0 4
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology 1 2 1 0 0 0 0 4
Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center 0 0 4 0 0 0 0 4
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 1 3 0 0 0 0 4
Athena Diagnostics 0 0 0 0 3 0 0 3
Service de Génétique Moléculaire, Hôpital Robert Debré 0 0 0 3 0 0 0 3
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille 1 1 1 0 0 0 0 3
Institute of Human Genetics, University Hospital of Duesseldorf 1 0 2 0 0 0 0 3
Undiagnosed Diseases Network, NIH 1 1 0 0 0 1 0 3
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 2 0 1 0 0 0 0 3
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 2 1 0 0 0 0 0 3
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital 0 0 2 1 0 0 0 3
Center of Excellence for Medical Genomics, Chulalongkorn University 2 1 0 0 0 0 0 3
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ 0 1 2 0 0 0 0 3
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein 0 2 1 0 0 0 0 3
Human Genetics Bochum, Ruhr University Bochum 0 1 2 0 0 0 0 3
Wen Jiang Lab, Comprehensive Epilepsy Center, Xijing Hospital 0 3 0 0 0 0 0 3
MVZ Medizinische Genetik Mainz 0 1 2 0 0 0 0 3
Genetic Services Laboratory, University of Chicago 1 0 1 0 0 0 0 2
Institute of Human Genetics, University of Goettingen 0 1 1 0 0 0 0 2
Duke University Health System Sequencing Clinic, Duke University Health System 0 2 0 0 0 0 0 2
Division of Human Genetics, Children's Hospital of Philadelphia 0 0 2 0 0 0 0 2
NeuroMeGen, Hospital Clinico Santiago de Compostela 0 2 0 0 0 0 0 2
Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin 0 0 2 0 0 0 0 2
Neurogenetics Laboratory - MEYER, AOU Meyer 0 0 2 0 0 0 0 2
Wangler Lab, Baylor College of Medicine 0 1 1 0 0 0 0 2
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard 0 0 1 0 1 0 0 2
Cavalleri Lab, Royal College of Surgeons in Ireland 1 0 1 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, 0 0 2 0 0 0 0 2
Clinical Genomics Laboratory, Stanford Medicine 0 0 2 0 0 0 0 2
Fondazione Telethon, Telethon Institute of Genetics and Medicine 2 0 0 0 0 0 0 2
Pediatric Genetics Clinic, Sheba Medical Center 0 1 1 0 0 0 0 2
Solve-RD Consortium 0 2 0 0 0 0 0 2
Medical Laboratory Center, Huzhou Maternal and Child Health Hospital 0 2 0 0 0 0 0 2
Servicio de Genética Del Instituto Nacional de Salud Del Niño, Ministerio de Salud 0 0 2 0 0 0 0 2
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet 0 1 0 0 0 0 0 1
Institute of Human Genetics, Cologne University 0 1 0 0 0 0 0 1
Centre for Inherited Metabolic Diseases, Karolinska University Hospital 1 0 0 0 0 0 0 1
Clinical Genomics Laboratory, Washington University in St. Louis 0 0 1 0 0 0 0 1
UCLA Clinical Genomics Center, UCLA 0 1 0 0 0 0 0 1
Clinical Genetics and Genomics, Karolinska University Hospital 1 0 0 0 0 0 0 1
Institute for Human Genetics and Genomic Medicine, Uniklinik RWTH Aachen 0 1 0 0 0 0 0 1
Institute of Experimental Medicine, Department of Genetics, Istanbul University 1 0 0 0 0 0 0 1
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine 0 1 0 0 0 0 0 1
Oxford Medical Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust 0 0 1 0 0 0 0 1
Gene Discovery Core-Manton Center, Boston Children's Hospital 1 0 0 0 0 0 0 1
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India 1 0 0 0 0 0 0 1
Fundacion Publica Galega de Medicina Xenomica, Servicio Galego de Saude 0 1 0 0 0 0 0 1
Institute of Medical Genetics, University of Zurich 0 1 0 0 0 0 0 1
Geisinger Autism and Developmental Medicine Institute, Geisinger Health System 0 0 1 0 0 0 0 1
Ambulatório de Genética Médica, Hospital Escola da Universidade Federal de Pelotas 0 1 0 0 0 0 0 1
Experimental Epileptology, AG Lerche, Hertie Institute for Clinical Brain Research 0 1 0 0 0 0 0 1
Center for Precision Medicine, Vanderbilt University Medical Center 0 0 1 0 0 0 0 1
HUSP Clinical Genetics Laboratory, Hospital Universitario San Pedro De Logroño (HUSP) 0 1 0 0 0 0 0 1
Genomic Medicine Lab, University of California San Francisco 0 1 0 0 0 0 0 1
Breda Genetics srl 0 0 1 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
Biochemistry Laboratory of CDMU, Chengde Medical University 1 0 0 0 0 0 0 1
Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn 0 1 0 0 0 0 0 1
Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan 0 0 1 0 0 0 0 1
Tianjin Key Laboratory of Birth Defects for Prevention and Treatment, Tianjin Children’s Hospital 0 1 0 0 0 0 0 1
Suma Genomics 1 0 0 0 0 0 0 1
DASA 0 1 0 0 0 0 0 1
Department of Neurology, Hunan Children's Hospital 1 0 0 0 0 0 0 1
Department of Neurology lab, Tongji Hospital, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology 1 0 0 0 0 0 0 1
Palindrome, Gene Kavoshgaran Aria 1 0 0 0 0 0 0 1
Developmental and Behavioral Pediatrics, First Affiliated Hospital of Jilin University 0 1 0 0 0 0 0 1
Key Laboratory of Neurobehavioral Science for Children, Children's Hospital Affiliated of Zhengzhou University 0 1 0 0 0 0 0 1
Institute of Immunology and Genetics Kaiserslautern 0 1 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 1
Pediatrics, Sichuan Provincial Hospital For Women And Children 0 1 0 0 0 0 0 1
Medical Genetic Diagnosis and Therapy Center, Fujian Medical University 0 1 0 0 0 0 0 1
Department of Developmental Neurology, Medical University of Gdańsk 0 0 0 0 0 0 1 1

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