List of variants in gene MSH6 reported as pathogenic for uterine corpus cancer

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.2759del (p.Lys920fs)	rs1114167794
NM_000179.3(MSH6):c.3477C>G (p.Tyr1159Ter)	rs398123231
NM_000179.3(MSH6):c.741dup (p.Arg248fs)	rs267608041

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