ClinVar Miner

Variants studied for infancy electroclinical syndrome

Included ClinVar conditions (46):
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
896 410 3902 3770 786 28 9579

Gene and significance breakdown #

Total genes and gene combinations: 105
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
SCN2A 209 117 715 621 81 8 1700
GRIN2B 46 33 346 517 159 1 1085
SIK1 5 2 417 417 83 0 909
CDKL5 294 101 218 244 74 1 892
PLCB1 14 14 428 416 49 0 884
PNKP 67 16 351 410 36 0 880
WWOX 50 13 298 250 45 0 654
TBC1D24 58 14 322 235 21 0 650
ARX 32 13 179 265 20 0 506
PIK3AP1 0 0 201 159 32 0 392
SPTAN1 16 36 129 57 126 1 335
MAF, WWOX 5 0 81 51 7 0 144
CDKL5, RS1 9 2 57 46 23 1 131
ARX, LOC109610631 14 3 44 61 9 1 126
SCN8A 8 16 26 3 9 2 63
MVP-DT, PRRT2 16 11 5 5 1 2 38
ST3GAL3 5 1 10 2 3 0 21
GUF1 1 1 5 0 6 0 13
LOC120977013, SCN2A 0 0 8 0 0 0 8
LOC130004439, PIK3AP1 0 0 5 3 0 0 8
KCNH5 6 0 0 0 0 0 6
KCNQ2 3 2 0 0 0 1 6
CACNA1A 0 1 3 0 0 0 4
CDKL5, LOC130067999 4 0 0 0 0 0 4
LOC130065408, PLCB1 0 0 3 0 1 0 4
SYNJ1 0 1 2 0 0 1 4
ARX, PCYT1B, PDK3, POLA1 1 0 2 0 0 0 3
BEND2, CDKL5, NHS, RAI2, RS1, SCML1, SCML2 1 0 2 0 0 0 3
LOC130004450, PIK3AP1 0 0 1 2 0 0 3
LOC130065410, PLCB1 0 0 1 1 1 0 3
MAST4 0 2 1 0 0 0 3
SCN1A 2 1 0 0 0 0 3
SCN2A, SCN3A 2 0 1 0 0 0 3
ABCG1, ADARB1, AGPAT3, AIRE, C21orf58, C2CD2, CBS, CFAP410, COL18A1, COL6A1, COL6A2, CRYAA, CSTB, DNMT3L, FTCD, GATD3, HSF2BP, ICOSLG, ITGB2, KRTAP10-1, KRTAP10-10, KRTAP10-11, KRTAP10-12, KRTAP10-2, KRTAP10-3, KRTAP10-4, KRTAP10-5, KRTAP10-6, KRTAP10-7, KRTAP10-8, KRTAP10-9, KRTAP12-1, KRTAP12-2, KRTAP12-3, KRTAP12-4, LINC00163, LINC00315, LINC00334, LRRC3, LSS, MCM3AP, NDUFV3, PCBP3, PCNT, PDE9A, PDXK, PFKL, PKNOX1, POFUT2, PRDM15, PTTG1IP, PWP2, RIPK4, RRP1, RRP1B, RSPH1, SIK1, SLC19A1, SLC37A1, SLX9, SPATC1L, SUMO3, TFF1, TFF2, TFF3, TMPRSS3, TRAPPC10, TRPM2, TSPEAR, U2AF1, UBASH3A, UBE2G2, UMODL1, WDR4, YBEY, ZBTB21 0 0 2 0 0 0 2
ADGRG2, BCLAF3, BEND2, CDKL5, EIF1AX, MAP3K15, MAP7D2, NHS, PDHA1, PHKA2, PPEF1, RAI2, RPS6KA3, RS1, SCML1, SCML2, SH3KBP1 1 0 1 0 0 0 2
AGPAT3, CSTB, GATD3, HSF2BP, PDXK, PWP2, RRP1, RRP1B, SIK1, TRAPPC10 1 0 1 0 0 0 2
ALDH7A1 0 0 2 0 0 0 2
ALG13 0 0 1 0 0 1 2
APOLD1, CDKN1B, DDX47, EMP1, FAM234B, GPRC5A, GPRC5D, GRIN2B, GSG1, HEBP1 1 0 1 0 0 0 2
ARHGEF9 0 0 0 0 0 2 2
ATP1A2 0 0 0 2 0 0 2
CCNF, TBC1D24 0 0 2 1 0 0 2
CSRNP3, GALNT3, SCN1A, SCN2A, SCN3A, SCN9A, TTC21B 1 0 1 0 0 0 2
CSRNP3, GALNT3, SCN1A, SCN2A, SCN9A, TTC21B 1 0 1 0 0 0 2
DNM1 1 0 0 0 0 1 2
KCNA2 0 2 0 0 0 1 2
LOC102724058, SCN1A 0 0 1 0 0 1 2
LOC112486209, LOC132090435, WWOX 1 1 0 0 0 0 2
LOC114803470, SCN8A 0 0 1 1 0 0 2
LOC120977013, LOC129935043, SCN2A, SCN3A 0 0 2 0 0 0 2
PACS2 1 0 1 0 0 0 2
STXBP1 1 1 0 0 0 0 2
ABCA3, BRICD5, CASKIN1, CCNF, DNASE1L2, E4F1, ECI1, EME2, FAHD1, GFER, HAGH, HS3ST6, IGFALS, MEIOB, MIR1225, MLST8, MRPS34, MSRB1, NDUFB10, NHERF2, NOXO1, NPW, NTHL1, NTN3, NUBP2, PGP, PKD1, RAB26, RNF151, RNPS1, RPL3L, RPS2, SNHG9, SPSB3, SYNGR3, TBC1D24, TBL3, TEDC2, TRAF7, TSC2, ZNF598 0 0 1 0 0 0 1
ABCA3, BRICD5, CASKIN1, CCNF, DNASE1L2, E4F1, ECI1, MIR1225, MLST8, NTN3, PGP, PKD1, RAB26, RNPS1, TBC1D24, TEDC2, TRAF7, TSC2 0 0 1 0 0 0 1
ACVR1B, ACVRL1, ANKRD33, FIGNL2, SCN8A 0 1 0 0 0 0 1
ADM5, AKT1S1, ALDH16A1, AP2A1, BCL2L12, CD37, CPT1C, DKKL1, FCGRT, FLT3LG, FUZ, IL4I1, IRF3, KASH5, MED25, MIR150, NOSIP, NUP62, PIH1D1, PNKP, PRMT1, PRR12, PRRG2, PTH2, PTOV1, RCN3, RPL13A, RPS11, RRAS, SCAF1, SLC17A7, SLC6A16, TBC1D17, TEAD2, TRPM4, TSKS 0 0 1 0 0 0 1
ADM5, ALDH16A1, AP2A1, BCL2L12, C19orf73, CD37, CGB1, CGB2, CGB3, CGB5, CGB7, CGB8, CPT1C, DKKL1, FCGRT, FLT3LG, FUZ, HRC, IRF3, KASH5, KCNA7, LHB, LIN7B, MED25, MIR150, NOSIP, NTF4, PIH1D1, PNKP, PPFIA3, PRMT1, PRR12, PRRG2, PTH2, PTOV1, RCN3, RPL13A, RPS11, RRAS, SCAF1, SLC17A7, SLC6A16, SNRNP70, TEAD2, TRPM4, TSKS 0 0 1 0 0 0 1
AGPAT3, CBS, CRYAA, CSTB, GATD3, HSF2BP, NDUFV3, PDE9A, PDXK, PKNOX1, PWP2, RRP1, RRP1B, RSPH1, SIK1, SLC37A1, TRAPPC10, U2AF1, WDR4 0 0 1 0 0 0 1
AGPAT3, CBS, CRYAA, CSTB, GATD3, HSF2BP, PDXK, PWP2, RRP1, RRP1B, SIK1, TRAPPC10, U2AF1 0 0 1 0 0 0 1
AMDHD2, ATP6V0C, BICDL2, CEMP1, CLDN6, CLDN9, ELOB, FLYWCH1, FLYWCH2, HCFC1R1, IL32, KCTD5, KREMEN2, MMP25, PAQR4, PDPK1, PKMYT1, PRSS21, PRSS22, PRSS27, PRSS33, PRSS41, SRRM2, TBC1D24, THOC6, TNFRSF12A, ZG16B, ZSCAN10 1 0 0 0 0 0 1
ANKEF1, HAO1, JAG1, LAMP5, MKKS, PAK5, PLCB1, PLCB4, SLX4IP, SNAP25, TMX4 1 0 0 0 0 0 1
APOLD1, ARHGDIB, ART4, ATF7IP, BCL2L14, BORCS5, C12orf60, CDKN1B, CREBL2, DDX47, DUSP16, EMP1, EPS8, ERP27, ETV6, FAM234B, GPR19, GPRC5A, GPRC5D, GRIN2B, GSG1, GUCY2C, H2AJ, H4C16, HEBP1, LRP6, MANSC1, MGP, PDE6H, PLBD1, PTPRO, RERG, SMCO3, WBP11 0 0 1 0 0 0 1
ARFGAP1, BIRC7, CHRNA4, COL20A1, EEF1A2, FNDC11, GMEB2, HELZ2, KCNQ2, NKAIN4, PPDPF, PTK6, RTEL1, SRMS, STMN3, YTHDF1 1 0 0 0 0 0 1
ARX, LOC110120595, LOC110120597, POLA1 0 0 1 0 0 0 1
ATMIN, BCO1, C16orf46, CDYL2, CENPN, CMC2, CMIP, DYNLRB2, GAN, GCSH, MAF, PKD1L2, PLCG2, WWOX 1 0 0 0 0 0 1
ATP6V1A 0 0 1 0 0 0 1
B3GALT1, CSRNP3, GALNT3, LOC100506124, LOC102724058, LOC120977013, LOC122847309, LOC126806396, LOC126806397, LOC129388938, LOC129935044, LOC129935045, LOC129935046, LOC129935047, LOC129935048, SCN1A, SCN2A, SCN7A, SCN9A, TTC21B, XIRP2 1 0 0 0 0 0 1
BEND2, CDKL5, NHS, RAI2, SCML1, SCML2 1 0 0 0 0 0 1
CDKL5, LOC121853052, LOC130067999 1 0 0 0 0 0 1
CFAP96, UFSP2 1 0 0 0 0 0 1
CHD2 0 0 0 0 0 1 1
CSNK1E, LOC126863148, TPTEP2-CSNK1E 1 0 0 0 0 0 1
CSRNP3, GALNT3, LOC100506124, LOC102724058, LOC120977013, LOC126806396, LOC129388938, LOC129935043, LOC129935044, LOC129935045, LOC129935046, LOC129935047, SCN1A, SCN2A, SCN3A, SCN9A, TTC21B 1 0 0 0 0 0 1
CSTB, HSF2BP, PDXK, RRP1B, SIK1 0 0 1 0 0 0 1
DYNC2I2, GLE1, SPTAN1 0 1 0 0 0 0 1
GABRB3 0 0 1 0 0 0 1
GAD1 0 0 1 0 0 0 1
GNAO1 0 1 0 0 0 0 1
GRIN1 0 1 0 0 0 0 1
HNRNPU 0 0 0 0 0 1 1
JMJD1C 0 0 0 1 0 0 1
KCNQ3 1 0 0 0 0 0 1
KCNT1 1 0 0 0 0 0 1
LOC110120570, LOC112486209, LOC121587562, LOC125177355, LOC132090428, LOC132090429, LOC132090430, LOC132090431, LOC132090432, LOC132090433, LOC132090434, LOC132090435, WWOX 0 0 1 0 0 0 1
LOC110120570, LOC112486209, LOC132090431, LOC132090432, LOC132090433, LOC132090434, LOC132090435, WWOX 0 0 1 0 0 0 1
LOC112486209, LOC132090431, LOC132090432, LOC132090433, LOC132090434, LOC132090435, WWOX 0 0 1 0 0 0 1
LOC125384577, PLCB1, RNU105B 0 0 1 0 0 0 1
LOC132090427, LOC132090428, LOC132090429, LOC132090888, WWOX 1 0 0 0 0 0 1
LOC132090428, LOC132090429, WWOX 0 0 1 0 0 0 1
LOC132090432, LOC132090433, LOC132090434, WWOX 1 0 0 0 0 0 1
MECP2 0 0 1 0 0 0 1
MED25, PNKP, PTOV1 1 0 0 0 0 0 1
NAPB 0 0 1 0 0 0 1
NRXN2 0 0 1 0 0 0 1
PCDH19 0 0 1 0 0 0 1
PRRT2 1 0 0 0 0 0 1
REPS2 0 0 1 0 0 0 1
SCN1B 0 0 0 0 0 1 1
SLC25A12 0 1 0 0 0 0 1
SLC2A1 1 0 0 0 0 0 1
SLC35A2 0 0 1 0 0 0 1
SNAP25 1 0 0 0 0 0 1
SZT2 0 0 1 0 0 0 1
TUBA1A 1 0 0 0 0 0 1
UGDH 0 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 125
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 616 187 3408 3653 597 0 8461
Genome-Nilou Lab 0 4 67 31 178 0 280
Illumina Laboratory Services, Illumina 0 0 161 28 56 0 245
Fulgent Genetics, Fulgent Genetics 6 2 52 35 5 0 100
Institute of Human Genetics, University of Leipzig Medical Center 24 30 32 3 1 0 90
RettBASE 75 8 4 0 0 0 87
Mendelics 37 19 5 4 8 0 73
OMIM 62 0 0 0 0 0 62
Genetic Services Laboratory, University of Chicago 26 5 27 0 0 0 58
Baylor Genetics 4 14 39 0 0 0 57
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 2 4 28 6 0 0 40
Neuberg Centre For Genomic Medicine, NCGM 4 6 29 0 0 0 39
Neurology Department, Shenzhen Children's Hospital 34 0 0 0 0 0 34
New York Genome Center 3 3 24 2 0 0 32
Génétique des Maladies du Développement, Hospices Civils de Lyon 16 9 2 4 0 0 31
Revvity Omics, Revvity 3 1 22 0 0 0 26
3billion 2 7 8 8 0 0 25
Genomic Research Center, Shahid Beheshti University of Medical Sciences 2 2 14 2 0 0 20
Laboratory of Inherited Metabolic Diseases, Research centre for medical genetics 11 2 5 0 0 0 18
Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan 8 7 3 0 0 0 18
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 6 3 5 2 0 0 16
MGZ Medical Genetics Center 4 4 6 0 0 0 14
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 2 12 0 0 0 14
NeuroMeGen, Hospital Clinico Santiago de Compostela 0 11 1 0 0 0 12
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 1 2 6 2 0 0 11
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille 6 5 0 0 0 0 11
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 0 5 6 0 11
GenomeConnect, ClinGen 0 0 0 0 0 10 10
GenomeConnect - Brain Gene Registry 0 0 0 0 0 10 10
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 2 6 0 0 0 0 8
Center for Human Genetics, Inc, Center for Human Genetics, Inc 0 4 1 1 1 0 7
Genome Diagnostics Laboratory, University Medical Center Utrecht 0 0 0 2 5 0 7
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 5 1 1 0 0 0 7
Solve-RD Consortium 0 7 0 0 0 0 7
Service de Génétique Moléculaire, Hôpital Robert Debré 2 4 0 0 0 0 6
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 2 2 2 0 0 0 6
Molecular Genetics Lab, CHRU Brest 2 2 2 0 0 0 6
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 4 2 0 0 0 6
Department of Neurology, Children’s Hospital of Chongqing Medical University 2 4 0 0 0 0 6
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 1 4 0 0 0 0 5
Centogene AG - the Rare Disease Company 2 1 2 0 0 0 5
MVZ Medizinische Genetik Mainz 0 3 2 0 0 0 5
Mayo Clinic Laboratories, Mayo Clinic 0 0 4 0 0 0 4
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München 3 1 0 0 0 0 4
Center of Genomic medicine, Geneva, University Hospital of Geneva 2 2 0 0 0 0 4
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues 0 1 3 0 0 0 4
Undiagnosed Diseases Network, NIH 3 1 0 0 0 0 4
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City 1 2 1 0 0 0 4
Center of Excellence for Medical Genomics, Chulalongkorn University 3 1 0 0 0 0 4
Diagnostic Genetics, Severance Hospital, Yonsei University College of Medicine 1 3 0 0 0 0 4
Pediatric Department, Xiangya Hospital, Central South University 4 0 0 0 0 0 4
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 4 4
Institute of Human Genetics, University of Goettingen 0 2 1 0 0 0 3
Institute for Genomic Medicine (IGM) Clinical Laboratory, Nationwide Children's Hospital 2 1 0 0 0 0 3
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 2 1 0 0 0 0 3
Clinical Genomics Laboratory, Washington University in St. Louis 0 0 3 0 0 0 3
Experimental Epileptology, AG Lerche, Hertie Institute for Clinical Brain Research 1 0 1 1 0 0 3
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard 0 3 0 0 0 0 3
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital 0 0 3 0 0 0 3
National Health Commission Key Laboratory of Birth Defects Research, Maternal and Child Health Hospital of Hunan 0 2 1 0 0 0 3
Key Laboratory of Neurobehavioral Science for Children, Children's Hospital Affiliated of Zhengzhou University 2 0 1 0 0 0 3
University of British Columbia, BC Children's Hospital 2 1 0 0 0 0 3
Athena Diagnostics 0 0 0 0 2 0 2
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital 0 0 2 0 0 0 2
Institute of Human Genetics, Cologne University 0 1 1 0 0 0 2
Centre for Inherited Metabolic Diseases, Karolinska University Hospital 1 0 1 0 0 0 2
GeneReviews 0 0 0 0 0 2 2
Dobyns Lab, Seattle Children's Research Institute 1 1 0 0 0 0 2
Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin 1 0 1 0 0 0 2
Institute of Human Genetics, University Hospital of Duesseldorf 1 0 1 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 2
Center for Molecular Medicine, Children’s Hospital of Fudan University 0 2 0 0 0 0 2
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 1 1 0 0 0 0 2
Department of Paediatrics and Adolescent Medicine, The University of Hong Kong 1 1 0 0 0 0 2
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology 0 1 1 0 0 0 2
Fondazione Telethon, Telethon Institute of Genetics and Medicine 2 0 0 0 0 0 2
Cell and Molecular Biology Laboratory, University of the Punjab Lahore 0 0 0 2 0 0 2
Lifecell International Pvt. Ltd 0 2 0 0 0 0 2
Pediatrics, MediClubGeorgia 1 1 0 0 0 0 2
Suma Genomics, Suma Genomics 1 0 0 1 0 0 2
Genomics England Pilot Project, Genomics England 0 2 0 0 0 0 2
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet 0 1 0 0 0 0 1
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 0 0 1 0 0 1
UniProtKB/Swiss-Prot 0 0 0 0 0 1 1
Blueprint Genetics 0 1 0 0 0 0 1
ITMI 1 0 0 0 0 0 1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 0 1 0 0 0 1
Gene Discovery Core-Manton Center, Boston Children's Hospital 0 1 0 0 0 0 1
Baylor-Hopkins Center for Mendelian Genomics, Johns Hopkins University School of Medicine 1 0 0 0 0 0 1
Molecular Genetics Department, Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology 0 1 0 0 0 0 1
Daryl Scott Lab, Baylor College of Medicine 0 1 0 0 0 0 1
Genetics and Molecular Pathology, SA Pathology 0 1 0 0 0 0 1
Groupe Hospitalier Pitie Salpetriere, UF Genomique du Developpement, Assistance Publique Hopitaux de Paris 1 0 0 0 0 0 1
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center 0 0 0 1 0 0 1
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota 0 1 0 0 0 0 1
UNC Molecular Genetics Laboratory, University of North Carolina at Chapel Hill 0 0 1 0 0 0 1
HUSP Clinical Genetics Laboratory, Hospital Universitario San Pedro De Logroño (HUSP) 0 1 0 0 0 0 1
Genomic Medicine Lab, University of California San Francisco 0 1 0 0 0 0 1
Kids Research, The Children's Hospital at Westmead 0 1 0 0 0 0 1
Laboratory of Medical Genetics, University of Torino 1 0 0 0 0 0 1
Wu Jinyu Laboratory, Institute of Genomic Medicine, Wenzhou Medical University 1 0 0 0 0 0 1
Johns Hopkins Genomics, Johns Hopkins University 0 0 1 0 0 0 1
Poduri Lab, Boston Children's Hospital 0 0 1 0 0 0 1
The Laboratory of Genetics and Metabolism, Hunan Children’s Hospital 0 1 0 0 0 0 1
Genetics Laboratory - UDIAT Centre Diagnòstic, Hospital Universitari Parc Tauli 0 1 0 0 0 0 1
GenomeConnect-Association for Creatine Deficiencies, Association for Creatine Deficiencies 0 0 0 0 0 1 1
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas 0 0 1 0 0 0 1
Molecular Medicine, University of Pavia 0 1 0 0 0 0 1
Genetics and Prenatal Diagnosis Center, The First Affiliated Hospital of Zhengzhou University 0 0 1 0 0 0 1
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ 0 0 0 1 0 0 1
Sydney Genome Diagnostics, Children's Hospital Westmead 1 0 0 0 0 0 1
Genomic Medicine, Universita Cattolica del Sacro Cuore 1 0 0 0 0 0 1
Beijing Key Laboratry for Genetics of Birth Defects, Beijing Children's Hospital 0 1 0 0 0 0 1
DASA 1 0 0 0 0 0 1
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein 1 0 0 0 0 0 1
Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg 1 0 0 0 0 0 1
Palindrome, Gene Kavoshgaran Aria 1 0 0 0 0 0 1
Developmental and Behavioral Pediatrics, First Affiliated Hospital of Jilin University 1 0 0 0 0 0 1
Institute of Immunology and Genetics Kaiserslautern 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 1
Payam Genetics Center, General Welfare Department of North Khorasan Province 1 0 0 0 0 0 1
Pediatrics, Sichuan Provincial Hospital For Women And Children 1 0 0 0 0 0 1
Medical Genetic Diagnosis and Therapy Center, Fujian Medical University 1 0 0 0 0 0 1
Watson Genetic Lab 0 1 0 0 0 0 1
Breakthrough Genomics, Breakthrough Genomics 1 0 0 0 0 0 1

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