List of variants in gene MSH6 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3647-6T>A	rs182871847	0.00134
NM_000179.3(MSH6):c.1526T>C (p.Val509Ala)	rs63751005	0.00067
NM_000179.3(MSH6):c.1665A>G (p.Ala555=)	rs146785465	0.00066
NM_000179.3(MSH6):c.663A>C (p.Glu221Asp)	rs41557217	0.00064
NM_000179.3(MSH6):c.1508C>G (p.Ser503Cys)	rs63750897	0.00059
NM_000179.3(MSH6):c.3245C>T (p.Pro1082Leu)	rs191109849	0.00010
NM_000179.3(MSH6):c.3399T>C (p.Thr1133=)	rs61748084	0.00005
NM_000179.3(MSH6):c.3729A>G (p.Thr1243=)	rs773807182	0.00004
NM_000179.3(MSH6):c.354A>G (p.Thr118=)	rs558590898	0.00002
NM_000179.3(MSH6):c.1524G>A (p.Val508=)	rs878853705	0.00001
NM_000179.3(MSH6):c.2940A>G (p.Glu980=)	rs730881818	0.00001
NM_000179.3(MSH6):c.3084A>T (p.Ser1028=)	rs786201843	0.00001
NM_000179.3(MSH6):c.81C>G (p.Ala27=)	rs781496151	0.00001
NM_000179.3(MSH6):c.2161A>C (p.Arg721=)	rs537604099
NM_000179.3(MSH6):c.2292T>C (p.Thr764=)	rs1553413668
NM_000179.3(MSH6):c.261-14C>T	rs369366445
NM_000179.3(MSH6):c.3162C>T (p.Ile1054=)	rs149605979
NM_000179.3(MSH6):c.3173-18T>A	rs189672273
NM_000179.3(MSH6):c.4001+2TAAC[2]	rs267608132

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