rs863225389

Orientation

plus

Stabilized

plus

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

Make rs863225389(-;-)

Make rs863225389(-;A)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47445573

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs863225389
dbSNP (classic)	rs863225389
ClinGen	rs863225389
ebi	rs863225389
HLI	rs863225389
Exac	rs863225389
Gnomad	rs863225389
Varsome	rs863225389
LitVar	rs863225389
Map	rs863225389
PheGenI	rs863225389
Biobank	rs863225389
1000 genomes	rs863225389
hgdp	rs863225389
ensembl	rs863225389
geneview	rs863225389
scholar	rs863225389
google	rs863225389
pharmgkb	rs863225389
gwascentral	rs863225389
openSNP	rs863225389
23andMe	rs863225389
SNPshot	rs863225389
SNPdbe	rs863225389
MSV3d	rs863225389
GWAS Ctlg	rs863225389

Max Magnitude

0

ClinVar
Risk	rs863225389(-;-)
Alt	rs863225389(-;-)
Reference	Rs863225389(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MSH2
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.47672712delA
CLNSRC
CLNACC	RCV000202110.1,