List of variants in gene MSH2 reported as uncertain significance for Breast carcinoma

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.435T>G (p.Ile145Met)	rs63750124	0.00031
NM_000251.3(MSH2):c.4G>A (p.Ala2Thr)	rs63750466	0.00008
NM_000251.3(MSH2):c.1571G>A (p.Arg524His)	rs63751207	0.00001
NM_000251.3(MSH2):c.1661+3T>G	rs1064793688
NM_000251.3(MSH2):c.2029A>G (p.Thr677Ala)	rs1553369013
NM_000251.3(MSH2):c.2697G>T (p.Met899Ile)	rs878853813

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