rs2744148

Orientation

plus

Stabilized

plus

Make rs2744148(A;A)

Make rs2744148(A;G)

Make rs2744148(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

1023552

is a	snp
is	mentioned by
dbSNP	rs2744148
dbSNP (classic)	rs2744148
ClinGen	rs2744148
ebi	rs2744148
HLI	rs2744148
Exac	rs2744148
Gnomad	rs2744148
Varsome	rs2744148
LitVar	rs2744148
Map	rs2744148
PheGenI	rs2744148
Biobank	rs2744148
1000 genomes	rs2744148
hgdp	rs2744148
ensembl	rs2744148
geneview	rs2744148
scholar	rs2744148
google	rs2744148
pharmgkb	rs2744148
gwascentral	rs2744148
openSNP	rs2744148
23andMe	rs2744148
SNPshot	rs2744148
SNPdbe	rs2744148
MSV3d	rs2744148
GWAS Ctlg	rs2744148

GMAF

0.1024

Max Magnitude

0

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

GWAS snp
PMID	[PMID 21833088]
Trait
Title	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele	G
P-val	8E-8
Odds Ratio	1.1200 [1.10-1.14]

[PMID 23739915] MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis

[PMID 29379819] Elevated EBNA-1 IgG in MS is associated with genetic MS risk variants.