MSH2[gene] AND Gln76His[varname] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 230330	NM_000251.3(MSH2):c.228G>C (p.Gln76His)	MSH2 (Q76H +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 142969	NM_000251.3(MSH2):c.228G>T (p.Gln76His)	MSH2 (Q76H +1 more)	Single nucleotide variant (missense variant)	Hereditary nonpolyposis colorectal neoplasms +3 more	GUncertain significance