ClinVar Miner

Variants studied for Arrhythmia

Coded as:
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
1 3 105 134 82 6 331

Gene and significance breakdown #

Total genes and gene combinations: 9
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
SCN5A 0 1 53 65 36 0 155
KCNH2 0 1 29 38 22 0 90
KCNQ1 0 1 21 21 16 0 59
LOC110121269, SCN5A 0 0 0 6 6 0 12
KCNQ1, KCNQ1OT1 0 0 1 4 2 0 7
ANK2 0 0 0 0 0 5 5
KCNA5 0 0 1 0 0 0 1
KCNJ2 0 0 0 0 0 1 1
SCN3B 1 0 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 5
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Color 0 2 102 134 82 0 320
Cardiovascular Biomedical Research Unit,Royal Brompton & Harefield NHS Foundation Trust 0 0 0 0 0 6 6
Centre for Mendelian Genomics,University Medical Centre Ljubljana 0 1 2 0 0 0 3
Forensic Genetics Laboratory,Harris County Institute of Forensic Sciences 1 0 0 0 0 0 1
CHLA Center for Personalized Medicine,Children's Hospital, Los Angeles 0 0 1 0 0 0 1

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