ClinVar Miner

List of variants studied for atrial fibrillation by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Included ClinVar conditions (49):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 13
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HGVS dbSNP gnomAD frequency
NM_002234.4(KCNA5):c.381C>T (p.Ser127=) rs45504599 0.02823
NM_002234.4(KCNA5):c.751G>A (p.Ala251Thr) rs12720442 0.01115
NM_002234.4(KCNA5):c.1733G>A (p.Arg578Lys) rs12720445 0.00612
NM_002234.4(KCNA5):c.929C>T (p.Pro310Leu) rs17215402 0.00439
NM_002234.4(KCNA5):c.570C>T (p.Asn190=) rs12720444 0.00368
NM_002234.4(KCNA5):c.919C>T (p.Pro307Ser) rs17215409 0.00241
NM_002234.4(KCNA5):c.634C>T (p.Arg212Cys) rs77281462 0.00088
NM_002234.4(KCNA5):c.1327A>G (p.Ile443Val) rs370591031 0.00010
NM_002234.4(KCNA5):c.544G>A (p.Gly182Arg) rs755408841 0.00008
NM_002234.4(KCNA5):c.1641G>T (p.Gly547=) rs1278466330
NM_002234.4(KCNA5):c.213_245del (p.Asp72_Pro82del) rs144879674
NM_002234.4(KCNA5):c.92G>T (p.Gly31Val) rs61737395
NM_004588.5(SCN2B):c.70+11_70+12insCT rs72544143

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