rs4792814

Orientation

plus

Stabilized

plus

Make rs4792814(C;C)

Make rs4792814(C;T)

Make rs4792814(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

45325639

is a	snp
is	mentioned by
dbSNP	rs4792814
dbSNP (classic)	rs4792814
ClinGen	rs4792814
ebi	rs4792814
HLI	rs4792814
Exac	rs4792814
Gnomad	rs4792814
Varsome	rs4792814
LitVar	rs4792814
Map	rs4792814
PheGenI	rs4792814
Biobank	rs4792814
1000 genomes	rs4792814
hgdp	rs4792814
ensembl	rs4792814
geneview	rs4792814
scholar	rs4792814
google	rs4792814
pharmgkb	rs4792814
gwascentral	rs4792814
openSNP	rs4792814
23andMe	rs4792814
SNPshot	rs4792814
SNPdbe	rs4792814
MSV3d	rs4792814
GWAS Ctlg	rs4792814

GMAF

0.4004

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 21833088]
Trait	Multiple sclerosis
Title	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele	G
P-val	3E-6
Odds Ratio	1.08 [1.06-1.09]