List of variants in gene MSH6 reported as uncertain significance by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3674C>T (p.Thr1225Met)	rs63750370	0.00011
NM_000179.3(MSH6):c.3283C>T (p.Arg1095Cys)	rs376243329	0.00006
NM_000179.3(MSH6):c.3703C>G (p.Leu1235Val)	rs876661084	0.00003
NM_000179.3(MSH6):c.3679A>T (p.Ile1227Leu)	rs587779282	0.00001
NM_000179.3(MSH6):c.1226G>A (p.Gly409Glu)	rs2104329429
NM_000179.3(MSH6):c.2045C>T (p.Ser682Phe)	rs587779225
NM_000179.3(MSH6):c.3259C>T (p.Pro1087Ser)	rs63750998
NM_000179.3(MSH6):c.779G>T (p.Gly260Val)	rs2104297173

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