List of variants in gene MSH6 reported as uncertain significance by Ding PR Lab, Sun Yat-sen University Cancer Center

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.2561A>T (p.Lys854Met)	rs34374438	0.00036
NM_000179.3(MSH6):c.3245C>T (p.Pro1082Leu)	rs191109849	0.00010
NM_000179.3(MSH6):c.1501C>T (p.His501Tyr)	rs779411998	0.00002
NM_000179.3(MSH6):c.1503T>G (p.His501Gln)	rs1572723237
NM_000179.3(MSH6):c.4001+2TAAC[2]	rs267608132
NM_000179.3(MSH6):c.4068_4071dup (p.Lys1358delinsAspTer)	rs55740729

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