List of variants in gene MSH2 reported as likely benign for breast disorder

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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: 23

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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.1277-8T>C	rs145400590	0.00159
NM_000251.3(MSH2):c.1563T>C (p.Tyr521=)	rs63750330	0.00053
NM_000251.3(MSH2):c.815C>T (p.Ala272Val)	rs34136999	0.00046
NM_000251.3(MSH2):c.1680T>C (p.Asn560=)	rs200056411	0.00043
NM_000251.3(MSH2):c.471C>A (p.Gly157=)	rs61756463	0.00029
NM_000251.3(MSH2):c.138C>G (p.His46Gln)	rs33946261	0.00019
NM_000251.3(MSH2):c.2425G>A (p.Glu809Lys)	rs202145681	0.00013
NM_000251.3(MSH2):c.505A>G (p.Ile169Val)	rs63750716	0.00013
NM_000251.3(MSH2):c.1386+23T>G	rs747646424	0.00010
NM_000251.3(MSH2):c.1560A>G (p.Gly520=)	rs63750820	0.00007
NM_000251.3(MSH2):c.2271C>T (p.Tyr757=)	rs56076152	0.00006
NM_000251.3(MSH2):c.2400A>G (p.Leu800=)	rs201298777	0.00006
NM_000251.3(MSH2):c.944G>T (p.Gly315Val)	rs202026056	0.00006
NM_000251.3(MSH2):c.2120G>A (p.Cys707Tyr)	rs373226409	0.00003
NM_000251.3(MSH2):c.399C>T (p.Asp133=)	rs61756462	0.00003
NM_000251.3(MSH2):c.1131A>G (p.Gln377=)	rs181852377	0.00002
NM_000251.3(MSH2):c.1759+9A>C	rs994093288	0.00001
NM_000251.3(MSH2):c.1760-12A>G	rs774350590	0.00001
NM_000251.3(MSH2):c.646-13T>C	rs761205332	0.00001
NM_000251.3(MSH2):c.2210+11_2210+22del	rs730881782
NM_000251.3(MSH2):c.67T>C (p.Phe23Leu)	rs372619120
NM_000251.3(MSH2):c.942+22_942+29del	rs11309117

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