List of variants in gene MSH6 reported as benign by Mayo Clinic Laboratories, Mayo Clinic

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3173-101G>C	rs2072447	0.78513
NM_000179.3(MSH6):c.3438+14A>T	rs2020911	0.32279
NM_000179.3(MSH6):c.540T>C (p.Asp180=)	rs1800935	0.23118
NM_000179.3(MSH6):c.116G>A (p.Gly39Glu)	rs1042821	0.18742
NM_000179.3(MSH6):c.276A>G (p.Pro92=)	rs1800932	0.14697
NM_000179.3(MSH6):c.186C>A (p.Arg62=)	rs1042820	0.12806
NM_000179.3(MSH6):c.628-56C>T	rs1800936	0.11629
NM_000179.3(MSH6):c.3172+171C>T	rs3136337	0.08328
NM_000179.3(MSH6):c.642C>T (p.Tyr214=)	rs1800937	0.07457
NM_000179.3(MSH6):c.2253T>C (p.Asn751=)	rs2020913	0.01882
NM_000179.3(MSH6):c.1164C>T (p.His388=)	rs55708305	0.01297
NM_000179.3(MSH6):c.2272C>T (p.Leu758=)	rs56371757	0.01274
NM_000179.3(MSH6):c.3306T>A (p.Thr1102=)	rs2020910	0.01157
NM_000179.3(MSH6):c.3557-40T>A	rs189436849	0.00576
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.1345C>T (p.Leu449=)	rs3136333	0.00394
NM_000179.3(MSH6):c.1508C>G (p.Ser503Cys)	rs63750897	0.00056
MSH6:c.3647-51_3647-35del17	rs267607687
NM_000179.3(MSH6):c.3173-94A>G	rs863225405
NM_000179.3(MSH6):c.3246G>T (p.Pro1082=)	rs3136351
NM_000179.3(MSH6):c.3557-4dup	rs267608102
NM_000179.3(MSH6):c.3646+35_3646+38del	rs1805181
NM_000179.3(MSH6):c.3646+91T>C	rs3136359
NM_000179.3(MSH6):c.3647-70TTTTTGTTTTAATTCCT[3]	rs267607687
NM_000179.3(MSH6):c.3759_3760insT (p.Glu1254Ter)	rs863225413
NM_000179.3(MSH6):c.3802-43dup	rs34154602
NM_000179.3(MSH6):c.3854dup (p.Leu1286fs)	rs863225415
NM_000179.3(MSH6):c.4002-10del	rs59056100

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