ClinVar Miner

List of variants in gene ANK2 studied for cardiac conduction defect

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.10901T>A (p.Val3634Asp) rs66785829 0.00200
NM_001148.6(ANK2):c.4373A>G (p.Glu1458Gly) rs72544141 0.00085
NM_001148.6(ANK2):c.2735A>G (p.His912Arg) rs139259028 0.00002
NM_001148.6(ANK2):c.9173G>A (p.Arg3058His) rs730880048 0.00001
NM_001148.6(ANK2):c.9245C>T (p.Thr3082Ile) rs770289485

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