ClinVar Miner

Variants studied for ventricular fibrillation

Included ClinVar conditions (16):
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
16 13 362 52 25 1 2 464

Gene and significance breakdown #

Total genes and gene combinations: 33
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign risk factor not provided total
SCN5A 13 7 292 39 15 0 2 362
LOC110121269, SCN5A 0 1 39 3 3 0 0 45
TTN 0 0 2 2 3 0 0 7
DPP6 0 0 3 0 2 1 0 6
AKAP9 0 0 2 1 1 0 0 4
DSP 1 0 3 0 0 0 0 4
CACNB2 0 0 2 1 0 0 0 3
RYR2 1 2 0 0 0 0 0 3
JUP 0 0 2 0 0 0 0 2
MYH7 0 0 0 2 0 0 0 2
PKP2 0 0 2 0 0 0 0 2
RBM20 0 0 2 0 0 0 0 2
SNTA1 0 0 2 0 0 0 0 2
ACTN2 0 0 1 0 0 0 0 1
ANK2 0 0 0 0 1 0 0 1
CACNA1C 0 1 0 0 0 0 0 1
CACNA2D1 0 1 0 0 0 0 0 1
DSG2 0 0 1 0 0 0 0 1
GAA 0 0 0 1 0 0 0 1
JPH2 0 0 1 0 0 0 0 1
KCNE3, LIPT2 0 0 1 0 0 0 0 1
KCNH2 0 0 1 0 0 0 0 1
KCNJ2 0 0 1 0 0 0 0 1
KCNQ1 0 0 0 1 0 0 0 1
LMNA, LOC129931597 0 0 1 0 0 0 0 1
LOC126806068, RYR2 0 1 0 0 0 0 0 1
LOC126861897, MHRT, MYH7 0 0 0 1 0 0 0 1
LOC130057222, TPM1 0 0 0 1 0 0 0 1
MYH6 0 0 1 0 0 0 0 1
NKX2-5 1 0 0 0 0 0 0 1
SCN1B 0 0 1 0 0 0 0 1
TRPM4 0 0 1 0 0 0 0 1
VCL 0 0 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 17
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign risk factor not provided total
Illumina Laboratory Services, Illumina 0 0 170 33 15 0 0 218
Fulgent Genetics, Fulgent Genetics 12 6 164 10 7 0 0 199
Blueprint Genetics 0 3 24 3 0 0 0 30
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 15 0 0 0 0 15
Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego 0 0 1 5 5 0 0 11
Agnes Ginges Centre for Molecular Cardiology, Centenary Institute 0 0 2 2 0 0 0 4
Centre for Mendelian Genomics, University Medical Centre Ljubljana 2 0 1 0 0 0 0 3
OMIM 1 0 0 0 0 1 0 2
Cardiovascular Biomedical Research Unit, Royal Brompton & Harefield NHS Foundation Trust 0 0 0 0 0 0 2 2
New York Genome Center 0 0 2 0 0 0 0 2
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 0 1 0 0 0 0 1
UCLA Clinical Genomics Center, UCLA 0 1 0 0 0 0 0 1
CSER _CC_NCGL, University of Washington 0 0 0 1 0 0 0 1
Scripps Translational Science Institute, Scripps Health and The Scripps Research Institute 1 0 0 0 0 0 0 1
Oxford Medical Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust 0 1 0 0 0 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 1 0 0 0 0 0 1
Division Of Personalized Genomic Medicine, Columbia University Irving Medical Center 0 1 0 0 0 0 0 1

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