List of variants in gene MSH6 reported as uncertain significance by Cancer Genomics Group, Japanese Foundation For Cancer Research

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.532C>T (p.Arg178Cys)	rs730881813	0.00003
NM_000179.3(MSH6):c.728G>A (p.Arg243His)	rs370157832	0.00002
NM_000179.3(MSH6):c.1190A>G (p.Tyr397Cys)	rs63750065	0.00001
NM_000179.3(MSH6):c.1660C>T (p.Arg554Cys)	rs775716798	0.00001
NM_000179.3(MSH6):c.233G>A (p.Arg78Lys)	rs864622425	0.00001
NM_000179.3(MSH6):c.1072G>A (p.Asp358Asn)	rs772747395
NM_000179.3(MSH6):c.1138G>A (p.Asp380Asn)	rs1064793521
NM_000179.3(MSH6):c.2226C>G (p.Asn742Lys)	rs587781739
NM_000179.3(MSH6):c.2297A>T (p.His766Leu)	rs1060502870
NM_000179.3(MSH6):c.230G>A (p.Arg77Gln)	rs1039603215
NM_000179.3(MSH6):c.2549A>C (p.Tyr850Ser)	rs63750389
NM_000179.3(MSH6):c.3143A>G (p.Gln1048Arg)	rs1572730351
NM_000179.3(MSH6):c.3151G>A (p.Val1051Ile)	rs576269342
NM_000179.3(MSH6):c.3689C>G (p.Ala1230Gly)	rs587782117
NM_000179.3(MSH6):c.4001+2TAAC[2]	rs267608132

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