ClinVar Miner

List of variants reported as risk factor for cardiomyopathy

Included ClinVar conditions (522):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_000363.5(TNNI3):c.244C>T (p.Pro82Ser) rs77615401 0.00699
NM_001943.5(DSG2):c.166G>A (p.Val56Met) rs121913013 0.00150
NM_006150.5(PRICKLE3):c.157C>T (p.Arg53Trp) rs2065470015 0.00002
NC_012920.1(MT-ND6):m.14502T>C rs201327354
NM_001818.5(AKR1C4):c.85-106G>T rs398122815

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