ClinVar Miner

List of variants in gene MSH6 reported as likely benign for Lynch syndrome I

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Total variants: 6
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HGVS dbSNP
NM_000179.2(MSH6):c.1487G>A (p.Cys496Tyr) rs764593111
NM_000179.2(MSH6):c.1508C>G (p.Ser503Cys) rs63750897
NM_000179.2(MSH6):c.1526T>C (p.Val509Ala) rs63751005
NM_000179.2(MSH6):c.2398G>C (p.Val800Leu) rs61748083
NM_000179.2(MSH6):c.3557-40T>A rs189436849
NM_000179.2(MSH6):c.59C>T (p.Ala20Val) rs63750664

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