List of variants in gene MSH6 reported as uncertain significance for Lynch-like syndrome

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.362G>A (p.Arg121His)	rs769279475	0.00003
NM_000179.3(MSH6):c.2419G>A (p.Glu807Lys)	rs587779923	0.00001
NM_000179.3(MSH6):c.1067G>A (p.Gly356Asp)	rs776170146
NM_000179.3(MSH6):c.1421T>C (p.Val474Ala)	rs1669329899
NM_000179.3(MSH6):c.2797T>C (p.Phe933Leu)	rs1553414155
NM_000179.3(MSH6):c.3039G>T (p.Lys1013Asn)	rs1060502920
NM_000179.3(MSH6):c.3222G>A (p.Met1074Ile)	rs1378407358
NM_000179.3(MSH6):c.3454G>A (p.Val1152Ile)	rs1572738396
NM_000179.3(MSH6):c.67G>A (p.Ala23Thr)	rs730881810

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