List of variants in gene SCN5A reported as likely benign by Blueprint Genetics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.6013C>G (p.Pro2005Ala)	rs45489199	0.00109
NM_000335.5(SCN5A):c.659C>T (p.Thr220Ile)	rs45620037	0.00068
NM_000335.5(SCN5A):c.568C>G (p.Arg190Gly)	rs199473068	0.00057
NM_000335.5(SCN5A):c.2074C>A (p.Gln692Lys)	rs45553235	0.00018
NM_000335.5(SCN5A):c.1715C>A (p.Ala572Asp)	rs36210423
NM_000335.5(SCN5A):c.5848G>T (p.Val1950Leu)	rs41315493

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