List of variants in gene MSH2 reported by Harris Lab, University of Minnesota

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000251.2(MSH2):c.*392G>A	rs104895029	0.00296
NM_000251.3(MSH2):c.1661+176A>G	rs104895025	0.00019
NM_000251.3(MSH2):c.874A>T (p.Thr292Ser)	rs104895022	0.00003
NM_000251.3(MSH2):c.1387-265A>G	rs104895024	0.00001
NM_000251.3(MSH2):c.367-108A>C	rs104895021	0.00001
NM_000251.2(MSH2):c.*387C>A	rs104895028
NM_000251.3(MSH2):c.*61T>A	rs104895027
NM_000251.3(MSH2):c.1076+176A>G	rs104895023
NM_000251.3(MSH2):c.2179G>T (p.Ala727Ser)	rs104895026

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