List of variants in gene MSH6 reported as benign for Breast and/or ovarian cancer

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3438+14A>T	rs2020911	0.32279
NM_000179.3(MSH6):c.2253T>C (p.Asn751=)	rs2020913	0.02003
NM_000179.3(MSH6):c.1186C>G (p.Leu396Val)	rs2020908	0.00565
NM_000179.3(MSH6):c.2633T>C (p.Val878Ala)	rs2020912	0.00448
NM_000179.3(MSH6):c.457+13A>G	rs1800933	0.00434
NM_000179.3(MSH6):c.1345C>T (p.Leu449=)	rs3136333	0.00429
NM_000179.3(MSH6):c.1526T>C (p.Val509Ala)	rs63751005	0.00067
NM_000179.3(MSH6):c.3172+20T>C	rs3136335	0.00009
NM_000179.3(MSH6):c.4002-10del	rs59056100
NM_000179.3(MSH6):c.4002-10dup	rs59056100
NM_000179.3(MSH6):c.4002-11_4002-10del	rs59056100
NM_000179.3(MSH6):c.4002-12_4002-10del	rs59056100
NM_000179.3(MSH6):c.4068_4071dup (p.Lys1358delinsAspTer)	rs55740729

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