ClinVar Miner

List of variants in gene MSH6 reported as likely pathogenic by Department of Pathology and Laboratory Medicine,Sinai Health System

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Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_000179.2(MSH6):c.1295T>C (p.Phe432Ser) rs750528093
NM_000179.2(MSH6):c.2314C>T (p.Arg772Trp) rs63750138
NM_000179.2(MSH6):c.3416G>T (p.Gly1139Val) rs1316409501
NM_000179.2(MSH6):c.3701_3706dup (p.Glu1234_Leu1235dup) rs63750523
NM_000179.2:c.1-?_260+?dup

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