rs630923

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs630923(A;A)

Make rs630923(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

118883644

Gene

CXCR5

is a	snp
is	mentioned by
dbSNP	rs630923
dbSNP (classic)	rs630923
ClinGen	rs630923
ebi	rs630923
HLI	rs630923
Exac	rs630923
Gnomad	rs630923
Varsome	rs630923
LitVar	rs630923
Map	rs630923
PheGenI	rs630923
Biobank	rs630923
1000 genomes	rs630923
hgdp	rs630923
ensembl	rs630923
geneview	rs630923
scholar	rs630923
google	rs630923
pharmgkb	rs630923
gwascentral	rs630923
openSNP	rs630923
23andMe	rs630923
SNPshot	rs630923
SNPdbe	rs630923
MSV3d	rs630923
GWAS Ctlg	rs630923

GMAF

0.1065

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	3E-7
Odds Ratio	1.1200 [1.10-1.14]

GWAS snp
PMID	[PMID 23128233 ]
Trait	Inflammatory bowel disease
Title	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele	C
P-val	7E-9
Odds Ratio	1.07 [1.039-1.11]

[PMID 23250934 ] Serum levels of the chemokine CXCL13, genetic variation in CXCL13 and its receptor CXCR5, and HIV-associated non-hodgkin B-cell lymphoma risk

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