rs863225385

Orientation

plus

Stabilized

plus

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

Make rs863225385(-;-)

Make rs863225385(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47429755

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs863225385
dbSNP (classic)	rs863225385
ClinGen	rs863225385
ebi	rs863225385
HLI	rs863225385
Exac	rs863225385
Gnomad	rs863225385
Varsome	rs863225385
LitVar	rs863225385
Map	rs863225385
PheGenI	rs863225385
Biobank	rs863225385
1000 genomes	rs863225385
hgdp	rs863225385
ensembl	rs863225385
geneview	rs863225385
scholar	rs863225385
google	rs863225385
pharmgkb	rs863225385
gwascentral	rs863225385
openSNP	rs863225385
23andMe	rs863225385
SNPshot	rs863225385
SNPdbe	rs863225385
MSV3d	rs863225385
GWAS Ctlg	rs863225385

Max Magnitude

0

ClinVar
Risk	rs863225385(-;-)
Alt	rs863225385(-;-)
Reference	Rs863225385(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MSH2
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.47656894delG
CLNSRC
CLNACC	RCV000202167.1,