List of variants in gene MSH2 reported as pathogenic 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.942+3A>T	rs193922376	0.00072
NM_000251.3(MSH2):c.1861C>T (p.Arg621Ter)	rs63750508
NM_000251.3(MSH2):c.204del (p.Pro69fs)	rs63750199
NM_000251.3(MSH2):c.229_230del (p.Ser77fs)	rs63749848
NM_000251.3(MSH2):c.387_388del (p.Gln130fs)	rs63750924
NM_000251.3(MSH2):c.482T>C (p.Val161Ala)	rs63750126

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