List of variants in gene MSH6 reported as not provided for not provided

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.-25C>T	rs1064793670	0.00004
NM_000179.3(MSH6):c.-6G>A	rs730881822
NM_000179.3(MSH6):c.1406A>G (p.Tyr469Cys)	rs748165218
NM_000179.3(MSH6):c.2337T>G (p.Cys779Trp)	rs1553413707
NM_000179.3(MSH6):c.2668G>T (p.Val890Phe)	rs786202628
NM_000179.3(MSH6):c.2956A>G (p.Thr986Ala)	rs1553414327
NM_000179.3(MSH6):c.3725G>A (p.Arg1242His)	rs63750119
NM_000179.3(MSH6):c.3989T>G (p.Leu1330Arg)	rs774395829

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