List of variants in gene MSH2 reported as pathogenic by Sema4, Sema4

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.942+3A>T	rs193922376	0.00072
NM_000251.3(MSH2):c.1906G>C (p.Ala636Pro)	rs63750875	0.00003
NM_000251.3(MSH2):c.1165C>T (p.Arg389Ter)	rs587779075
NM_000251.3(MSH2):c.1861C>T (p.Arg621Ter)	rs63750508
NM_000251.3(MSH2):c.2113del (p.Val705fs)	rs63749811
NM_000251.3(MSH2):c.484G>A (p.Gly162Arg)	rs63750624
NM_000251.3(MSH2):c.998G>A (p.Cys333Tyr)	rs63750828

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