List of variants in gene MSH2 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.1077-225G>A	rs192783837	0.00526
NM_000251.3(MSH2):c.499G>C (p.Asp167His)	rs63750255	0.00006
NC_000002.12:g.47402579G>T

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