List of variants in gene MSH6 reported as benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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.3802-40C>G	rs3136367	0.73398
NM_000179.3(MSH6):c.3438+14A>T	rs2020911	0.32279
NM_000179.3(MSH6):c.457+52T>A	rs3136282	0.29585
NM_000179.3(MSH6):c.540T>C (p.Asp180=)	rs1800935	0.23857
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.642C>T (p.Tyr214=)	rs1800937	0.07457
NM_000179.3(MSH6):c.3306T>A (p.Thr1102=)	rs2020910	0.00869
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.3439-16C>T	rs192614006	0.00237
NM_000179.3(MSH6):c.1053C>T (p.His351=)	rs28903083	0.00003
NM_000179.3(MSH6):c.3246G>T (p.Pro1082=)	rs3136351
NM_000179.3(MSH6):c.3646+35_3646+38del	rs1805181
NM_000179.3(MSH6):c.4001+2TAAC[4]	rs267608132
NM_000179.3(MSH6):c.4002-10del	rs59056100
NM_000179.3(MSH6):c.4002-10dup	rs59056100

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