List of variants in gene SCN5A reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.2263-18T>C	rs9835588	0.02184
NM_000335.5(SCN5A):c.482+16G>C	rs41312949	0.01894
NM_000335.5(SCN5A):c.4215G>A (p.Gly1405=)	rs41311123	0.00859
NM_000335.5(SCN5A):c.1587T>C (p.Ile529=)	rs45624133	0.00575
NM_000335.5(SCN5A):c.3508+10C>T	rs41258454	0.00510
NM_000335.5(SCN5A):c.717C>T (p.Ile239=)	rs41285129	0.00407
NM_000335.5(SCN5A):c.4434+13C>T	rs148598985	0.00361
NM_000335.5(SCN5A):c.4506C>T (p.Ser1502=)	rs45548237	0.00350
NM_000335.5(SCN5A):c.2436+12G>A	rs41312419	0.00284
NM_000335.5(SCN5A):c.486C>T (p.Tyr162=)	rs45489099	0.00267
NM_000335.5(SCN5A):c.1890+14G>A	rs145427253	0.00252
NM_000335.5(SCN5A):c.4821C>T (p.Leu1607=)	rs45437099	0.00242
NM_000335.5(SCN5A):c.1681C>T (p.Leu561=)	rs45522138	0.00196
NM_000335.5(SCN5A):c.1852C>T (p.Leu618Phe)	rs45488304	0.00178
NM_000335.5(SCN5A):c.4297-14T>C	rs56104887	0.00117
NM_000335.5(SCN5A):c.1236C>T (p.Val412=)	rs45565936	0.00114
NM_000335.5(SCN5A):c.2437-13C>T	rs45455099	0.00076
NM_000335.5(SCN5A):c.647C>T (p.Ser216Leu)	rs41276525	0.00065
NM_000335.5(SCN5A):c.630G>A (p.Val210=)	rs193922727	0.00064
NM_000335.5(SCN5A):c.2437-5C>A	rs72549411	0.00045
NM_000335.5(SCN5A):c.1044C>T (p.Pro348=)	rs370346797	0.00043
NM_000335.5(SCN5A):c.1008G>A (p.Pro336=)	rs200285003	0.00042
NM_000335.5(SCN5A):c.3748G>A (p.Val1250Met)	rs199473600	0.00038
NM_000335.5(SCN5A):c.5709G>A (p.Ser1903=)	rs376826051	0.00034
NM_000335.5(SCN5A):c.3388-16A>T	rs376625229	0.00029
NM_000335.5(SCN5A):c.3837+17G>A	rs45466091	0.00029
NM_000335.5(SCN5A):c.1152C>T (p.Ser384=)	rs372970828	0.00011
NM_000335.5(SCN5A):c.*1G>A	rs375282305	0.00010
NM_000335.5(SCN5A):c.2103G>A (p.Pro701=)	rs564847999	0.00009
NM_000335.5(SCN5A):c.3951G>A (p.Glu1317=)	rs769473892	0.00009
NM_000335.5(SCN5A):c.3508+11G>A	rs200058362	0.00003
NM_000335.5(SCN5A):c.1715C>A (p.Ala572Asp)	rs36210423
NM_000335.5(SCN5A):c.5848G>T (p.Val1950Leu)	rs41315493

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