List of variants in gene MSH6 reported as likely pathogenic by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3226C>T (p.Arg1076Cys)	rs63750617	0.00002
NM_000179.3(MSH6):c.2222dup (p.Asn741fs)
NM_000179.3(MSH6):c.3697_3733dup (p.Phe1245Ter)
NM_000179.3(MSH6):c.461C>G (p.Ser154Ter)	rs1553411391
NM_000179.3(MSH6):c.936_945del (p.Lys313fs)

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