List of variants in gene MSH6 reported as uncertain significance 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.2561A>T (p.Lys854Met)	rs34374438	0.00036
NM_000179.3(MSH6):c.3245C>T (p.Pro1082Leu)	rs191109849	0.00010
NM_000179.3(MSH6):c.2384T>C (p.Ile795Thr)	rs202127474	0.00007
NM_000179.3(MSH6):c.1501C>T (p.His501Tyr)	rs779411998	0.00002
NM_000179.3(MSH6):c.1106C>T (p.Thr369Ile)	rs375974046	0.00001
NM_000179.3(MSH6):c.1503T>G (p.His501Gln)	rs1572723237
NM_000179.3(MSH6):c.2782A>G (p.Thr928Ala)	rs1057519255
NM_000179.3(MSH6):c.3556+5_3556+8delinsCATTATTGTCAGG	rs2104510542
NM_000179.3(MSH6):c.4001+2TAAC[2]	rs267608132
NM_000179.3(MSH6):c.4072A>G (p.Lys1358Glu)	rs199739099
NM_000179.3(MSH6):c.726C>A (p.Ser242Arg)	rs1553412151

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