List of variants in gene MSH2 reported as pathogenic for female reproductive organ cancer

Minimum submission review status:		Collection method:
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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.1163dup (p.Asn388fs)	rs2104439295
NM_000251.3(MSH2):c.1500dup (p.Arg501fs)	rs587779094
NM_000251.3(MSH2):c.1566C>G (p.Tyr522Ter)	rs63750224
NM_000251.3(MSH2):c.1661+5G>C	rs267607972
NM_000251.3(MSH2):c.1676del (p.Ser558_Leu559insTer)	rs63750633
NM_000251.3(MSH2):c.1720del (p.Gln574fs)	rs63751299
NM_000251.3(MSH2):c.1738G>T (p.Glu580Ter)	rs63751411
NM_000251.3(MSH2):c.2267_2268insGTAG (p.Thr756_Tyr757insTer)	rs1558521605
NM_000251.3(MSH2):c.367-2_645+742del
NM_000251.3(MSH2):c.459del (p.Ala154fs)	rs2104023773
NM_000251.3(MSH2):c.508C>T (p.Gln170Ter)	rs63750843
NM_000251.3(MSH2):c.811_814del (p.Ser271fs)	rs587779185

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