List of variants in gene MSH6 reported as benign by Genome Diagnostics Laboratory, University Medical Center Utrecht

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.642C>T (p.Tyr214=)	rs1800937	0.07457
NM_000179.3(MSH6):c.2633T>C (p.Val878Ala)	rs2020912	0.00448
NM_000179.3(MSH6):c.3439-16C>T	rs192614006	0.00237
NM_000179.3(MSH6):c.1049C>T (p.Ala350Val)	rs587782331	0.00003
NM_000179.3(MSH6):c.3557-4dup	rs267608102
NM_000179.3(MSH6):c.4002-10del	rs59056100
NM_000179.3(MSH6):c.4002-10dup	rs59056100

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