rs12466022

Orientation

plus

Stabilized

plus

Make rs12466022(A;A)

Make rs12466022(A;C)

Make rs12466022(C;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

43131922

Gene	LOC100506047, LOC105374570

is a	snp
is	mentioned by
dbSNP	rs12466022
dbSNP (classic)	rs12466022
ClinGen	rs12466022
ebi	rs12466022
HLI	rs12466022
Exac	rs12466022
Gnomad	rs12466022
Varsome	rs12466022
LitVar	rs12466022
Map	rs12466022
PheGenI	rs12466022
Biobank	rs12466022
1000 genomes	rs12466022
hgdp	rs12466022
ensembl	rs12466022
geneview	rs12466022
scholar	rs12466022
google	rs12466022
pharmgkb	rs12466022
gwascentral	rs12466022
openSNP	rs12466022
23andMe	rs12466022
SNPshot	rs12466022
SNPdbe	rs12466022
MSV3d	rs12466022
GWAS Ctlg	rs12466022

GMAF

0.3044

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

GWAS snp
PMID	[PMID 21833088]
Trait
Title	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele	C
P-val	6E-10
Odds Ratio	1.1100 1.10-1.13]