rs1064794075

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(TA;TA)	0	common in clinvar

Chromosome

2

Position

47783495

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1064794075
dbSNP (classic)	rs1064794075
ClinGen	rs1064794075
ebi	rs1064794075
HLI	rs1064794075
Exac	rs1064794075
Gnomad	rs1064794075
Varsome	rs1064794075
LitVar	rs1064794075
Map	rs1064794075
PheGenI	rs1064794075
Biobank	rs1064794075
1000 genomes	rs1064794075
hgdp	rs1064794075
ensembl	rs1064794075
geneview	rs1064794075
scholar	rs1064794075
google	rs1064794075
pharmgkb	rs1064794075
gwascentral	rs1064794075
openSNP	rs1064794075
23andMe	rs1064794075
SNPshot	rs1064794075
SNPdbe	rs1064794075
MSV3d	rs1064794075
GWAS Ctlg	rs1064794075

Max Magnitude

0

ClinVar
Risk	rs1064794075(AG;AG)
Alt	rs1064794075(AG;AG)
Reference	Rs1064794075(TA;TA)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48010634_48010635delTAinsAG
CLNSRC
CLNACC	RCV000479300.1, RCV000491081.1,