rs1064794155

Orientation

plus

Stabilized

plus

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

Chromosome

2

Position

47412561

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs1064794155
dbSNP (classic)	rs1064794155
ClinGen	rs1064794155
ebi	rs1064794155
HLI	rs1064794155
Exac	rs1064794155
Gnomad	rs1064794155
Varsome	rs1064794155
LitVar	rs1064794155
Map	rs1064794155
PheGenI	rs1064794155
Biobank	rs1064794155
1000 genomes	rs1064794155
hgdp	rs1064794155
ensembl	rs1064794155
geneview	rs1064794155
scholar	rs1064794155
google	rs1064794155
pharmgkb	rs1064794155
gwascentral	rs1064794155
openSNP	rs1064794155
23andMe	rs1064794155
SNPshot	rs1064794155
SNPdbe	rs1064794155
MSV3d	rs1064794155
GWAS Ctlg	rs1064794155

Max Magnitude

0

ClinVar
Risk	rs1064794155(-;-)
Alt	rs1064794155(-;-)
Reference	Rs1064794155(G;G)
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.47639700delG
CLNSRC
CLNACC	RCV000485573.1, RCV000491720.1,