List of variants in gene MSH6 reported as likely benign by Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C.

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.457+13A>G	rs1800933	0.00434
NM_000179.3(MSH6):c.1508C>G (p.Ser503Cys)	rs63750897	0.00059
NM_000179.3(MSH6):c.4001+11_4001+15dup	rs587779302	0.00019
NM_000179.3(MSH6):c.3160A>T (p.Ile1054Phe)	rs267608075	0.00016
NM_000179.3(MSH6):c.628-7C>A	rs373129248	0.00011
NM_000179.3(MSH6):c.178T>C (p.Leu60=)	rs35819209	0.00006
NM_000179.3(MSH6):c.147C>T (p.Ala49=)	rs768803986	0.00005
NM_000179.3(MSH6):c.81C>G (p.Ala27=)	rs781496151	0.00001
NM_000179.3(MSH6):c.1806A>G (p.Ser602=)	rs1057520981
NM_000179.3(MSH6):c.2403G>T (p.Val801=)	rs1572727035
NM_000179.3(MSH6):c.3438+6T>G

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