rs876660480

Orientation

plus

Stabilized

plus

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

Make rs876660480(-;-)

Make rs876660480(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47403351

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs876660480
dbSNP (classic)	rs876660480
ClinGen	rs876660480
ebi	rs876660480
HLI	rs876660480
Exac	rs876660480
Gnomad	rs876660480
Varsome	rs876660480
LitVar	rs876660480
Map	rs876660480
PheGenI	rs876660480
Biobank	rs876660480
1000 genomes	rs876660480
hgdp	rs876660480
ensembl	rs876660480
geneview	rs876660480
scholar	rs876660480
google	rs876660480
pharmgkb	rs876660480
gwascentral	rs876660480
openSNP	rs876660480
23andMe	rs876660480
SNPshot	rs876660480
SNPdbe	rs876660480
MSV3d	rs876660480
GWAS Ctlg	rs876660480

Max Magnitude

0

ClinVar
Risk	rs876660480(-;-)
Alt	rs876660480(-;-)
Reference	Rs876660480(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47630490delG
CLNSRC
CLNACC	RCV000213902.1,