ClinVar Miner

Variants from Roden Lab, Vanderbilt University Medical Center

Location: United States  Primary collection method: in vitro
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:

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
2 19 36 31 0 1106 1194

Gene and significance breakdown #

Total genes and gene combinations: 6
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign not provided total
KCNE1 0 0 0 0 1106 1106
SCN5A 0 13 34 31 0 78
KCNQ1 1 3 1 0 0 5
KCNH2 0 3 0 0 0 3
FLNC 1 0 0 0 0 1
LOC110121269, SCN5A 0 0 1 0 0 1

Condition and significance breakdown #

Total conditions: 5
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Condition pathogenic likely pathogenic uncertain significance likely benign not provided total
Long QT syndrome 5 0 0 0 0 1106 1106
Brugada syndrome 1 0 13 35 31 0 79
Long QT syndrome 1 1 3 1 0 0 5
Long QT syndrome 2 0 3 0 0 0 3
Arrhythmogenic right ventricular cardiomyopathy 1 0 0 0 0 1

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