List of variants reported as uncertain significance for Ventricular fibrillation by Blueprint Genetics

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_017636.4(TRPM4):c.1682A>C (p.Asp561Ala)	rs56355369	0.00373
NM_001037.5(SCN1B):c.448+112G>A	rs72558026	0.00049
NM_000891.3(KCNJ2):c.973C>T (p.Arg325Cys)	rs202067116	0.00007
NM_201596.3(CACNB2):c.334-8C>T	rs374465425	0.00006
NM_002471.4(MYH6):c.2612G>A (p.Arg871His)	rs869025473	0.00004
NM_004415.4(DSP):c.3134G>A (p.Arg1045Gln)	rs374263890	0.00004
NM_003098.3(SNTA1):c.1210G>A (p.Ala404Thr)	rs730880217	0.00001
NM_201596.3(CACNB2):c.1056G>A (p.Ala352=)	rs730880058	0.00001
NM_001005242.3(PKP2):c.964G>T (p.Gly322Cys)	rs200069860
NM_001103.4(ACTN2):c.82C>T (p.Arg28Cys)	rs730880040
NM_001943.5(DSG2):c.3265G>A (p.Gly1089Ser)	rs869025389
NM_005751.5(AKAP9):c.4825_4826delinsCA (p.Arg1609Gln)	rs786205707
NM_005751.5(AKAP9):c.5272G>C (p.Asp1758His)	rs142603711

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