List of variants in gene MSH6 reported as likely pathogenic for Carcinoma of colon

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.2504del (p.Gln835fs)	rs1572727440	0.00001
NM_000179.3(MSH6):c.2300C>T (p.Thr767Ile)	rs587781462
NM_000179.3(MSH6):c.2314C>T (p.Arg772Trp)	rs63750138
NM_000179.3(MSH6):c.3477C>A (p.Tyr1159Ter)	rs398123231
NM_000179.3(MSH6):c.3557-3_3573del	rs2104521349
NM_000179.3(MSH6):c.3701_3706dup (p.Glu1234_Leu1235dup)	rs63750523

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