List of variants in gene MSH6 reported as pathogenic for Lynch syndrome 1

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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: 12

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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.467C>G (p.Ser156Ter)	rs63749873	0.00001
NM_000179.3(MSH6):c.1100A>G (p.His367Arg)	rs1553412495
NM_000179.3(MSH6):c.1135_1139del (p.Arg378_Arg379insTer)	rs267608077
NM_000179.3(MSH6):c.1705_1706del (p.Phe569fs)	rs587783056
NM_000179.3(MSH6):c.2062_2063del (p.Val688fs)	rs63750075
NM_000179.3(MSH6):c.2300C>T (p.Thr767Ile)	rs587781462
NM_000179.3(MSH6):c.2873_2874del (p.Gln958fs)	rs1553414239
NM_000179.3(MSH6):c.3188T>G (p.Leu1063Arg)	rs1060502901
NM_000179.3(MSH6):c.3477C>G (p.Tyr1159Ter)	rs398123231
NM_000179.3(MSH6):c.426G>A (p.Trp142Ter)	rs63750342
NM_000179.3(MSH6):c.718C>T (p.Arg240Ter)	rs63750019

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