rs1064794809

Orientation

plus

Stabilized

plus

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

Chromosome

2

Position

47414347

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs1064794809
dbSNP (classic)	rs1064794809
ClinGen	rs1064794809
ebi	rs1064794809
HLI	rs1064794809
Exac	rs1064794809
Gnomad	rs1064794809
Varsome	rs1064794809
LitVar	rs1064794809
Map	rs1064794809
PheGenI	rs1064794809
Biobank	rs1064794809
1000 genomes	rs1064794809
hgdp	rs1064794809
ensembl	rs1064794809
geneview	rs1064794809
scholar	rs1064794809
google	rs1064794809
pharmgkb	rs1064794809
gwascentral	rs1064794809
openSNP	rs1064794809
23andMe	rs1064794809
SNPshot	rs1064794809
SNPdbe	rs1064794809
MSV3d	rs1064794809
GWAS Ctlg	rs1064794809

Max Magnitude

0

ClinVar
Risk	rs1064794809(-;-)
Alt	rs1064794809(-;-)
Reference	Rs1064794809(C;C)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47641486delC
CLNSRC
CLNACC	RCV000484912.1, RCV000491867.1,