rs1064795653

Orientation

plus

Stabilized

plus

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

Chromosome

2

Position

47466717

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs1064795653
dbSNP (classic)	rs1064795653
ClinGen	rs1064795653
ebi	rs1064795653
HLI	rs1064795653
Exac	rs1064795653
Gnomad	rs1064795653
Varsome	rs1064795653
LitVar	rs1064795653
Map	rs1064795653
PheGenI	rs1064795653
Biobank	rs1064795653
1000 genomes	rs1064795653
hgdp	rs1064795653
ensembl	rs1064795653
geneview	rs1064795653
scholar	rs1064795653
google	rs1064795653
pharmgkb	rs1064795653
gwascentral	rs1064795653
openSNP	rs1064795653
23andMe	rs1064795653
SNPshot	rs1064795653
SNPdbe	rs1064795653
MSV3d	rs1064795653
GWAS Ctlg	rs1064795653

Max Magnitude

0

ClinVar
Risk	rs1064795653(-;-)
Alt	rs1064795653(-;-)
Reference	Rs1064795653(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MSH2
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.47693856delC
CLNSRC
CLNACC	RCV000481233.1,