List of variants in gene MSH6 reported as likely pathogenic by Sema4, Sema4

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: 6

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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.171del (p.Arg58fs)	rs1553408306
NM_000179.3(MSH6):c.2300C>T (p.Thr767Ile)	rs587781462
NM_000179.3(MSH6):c.3163dup (p.Ala1055fs)	rs878853729
NM_000179.3(MSH6):c.3646+2del	rs2104526796
NM_000179.3(MSH6):c.3815_3816insT (p.Glu1272fs)	rs2104552191

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