rs4669226

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0

Make rs4669226(A;G)

Make rs4669226(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

7913466

is a	snp
is	mentioned by
dbSNP	rs4669226
dbSNP (classic)	rs4669226
ClinGen	rs4669226
ebi	rs4669226
HLI	rs4669226
Exac	rs4669226
Gnomad	rs4669226
Varsome	rs4669226
LitVar	rs4669226
Map	rs4669226
PheGenI	rs4669226
Biobank	rs4669226
1000 genomes	rs4669226
hgdp	rs4669226
ensembl	rs4669226
geneview	rs4669226
scholar	rs4669226
google	rs4669226
pharmgkb	rs4669226
gwascentral	rs4669226
openSNP	rs4669226
23andMe	rs4669226
SNPshot	rs4669226
SNPdbe	rs4669226
MSV3d	rs4669226
GWAS Ctlg	rs4669226

GMAF

0.03994

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 23412934]
Trait	Multiple sclerosis
Title	A genome-wide association study of brain lesion distribution in multiple sclerosis.
Risk Allele
P-val	5E-6
Odds Ratio	NR NR