List of variants in gene MSH6 reported as pathogenic for Lynch-like syndrome

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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.3202C>T (p.Arg1068Ter)	rs63749843	0.00002
NM_000179.3(MSH6):c.1159del (p.Asp387fs)	rs1669301838
NM_000179.3(MSH6):c.1483C>T (p.Arg495Ter)	rs587779212
NM_000179.3(MSH6):c.1721C>G (p.Ser574Ter)	rs1669365820
NM_000179.3(MSH6):c.1767del (p.Pro591fs)	rs1114167765
NM_000179.3(MSH6):c.1819del (p.Thr607fs)	rs587779221
NM_000179.3(MSH6):c.2079del (p.Lys693fs)	rs267608083
NM_000179.3(MSH6):c.2629G>T (p.Glu877Ter)	rs730881797
NM_000179.3(MSH6):c.2677_2678del (p.Leu893fs)	rs1572728112
NM_000179.3(MSH6):c.2719del (p.Thr906_Val907insTer)	rs1669502158
NM_000179.3(MSH6):c.2836G>T (p.Glu946Ter)	rs1558666905
NM_000179.3(MSH6):c.3141G>A (p.Trp1047Ter)	rs1553414554
NM_000179.3(MSH6):c.3261_3262del (p.Phe1088fs)	rs1669747095
NM_000179.3(MSH6):c.3261del (p.Phe1088fs)	rs267608078
NM_000179.3(MSH6):c.3261dup (p.Phe1088fs)	rs267608078
NM_000179.3(MSH6):c.3416dup (p.Lys1140fs)	rs587781544
NM_000179.3(MSH6):c.3477C>A (p.Tyr1159Ter)	rs398123231
NM_000179.3(MSH6):c.3724_3726del (p.Arg1242del)	rs63749942
NM_000179.3(MSH6):c.3964G>T (p.Glu1322Ter)	rs1553333707

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