List of variants in gene SCN10A reported as likely benign for Brugada syndrome

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 15

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HGVS	dbSNP
NM_006514.3(SCN10A):c.1641C>A (p.Gly547=)	rs1444054143
NM_006514.3(SCN10A):c.1959G>A (p.Lys653=)	rs1217257967
NM_006514.3(SCN10A):c.2484C>T (p.Pro828=)	rs777634572
NM_006514.3(SCN10A):c.2499C>T (p.His833=)	rs995722247
NM_006514.3(SCN10A):c.3705G>A (p.Ala1235=)	rs147376215
NM_006514.3(SCN10A):c.3711T>A (p.Ile1237=)	rs148339462
NM_006514.3(SCN10A):c.3759C>T (p.Arg1253=)	rs749134108
NM_006514.3(SCN10A):c.3870C>A (p.Ile1290=)	rs1371664893
NM_006514.3(SCN10A):c.4063A>G (p.Met1355Val)	rs375458594
NM_006514.3(SCN10A):c.4128T>C (p.Ala1376=)	rs1060504317
NM_006514.3(SCN10A):c.4137C>A (p.Ser1379=)	rs779905648
NM_006514.3(SCN10A):c.4173C>T (p.Asn1391=)	rs374352107
NM_006514.3(SCN10A):c.4584C>T (p.Phe1528=)	rs141828577
NM_006514.3(SCN10A):c.470+7A>G	rs1173885296
NM_006514.3(SCN10A):c.5286T>C (p.Ser1762=)	rs750340252

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