List of variants in gene MSH2 reported as likely benign for Breast carcinoma

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.965G>A (p.Gly322Asp)	rs4987188	0.01714
NM_000251.3(MSH2):c.1386+23T>G	rs747646424	0.00010
NM_000251.3(MSH2):c.942+22_942+29del	rs11309117

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