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rs630923

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs630923(A;A)
Make rs630923(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position118883644
GeneCXCR5
is asnp
is mentioned by
dbSNPrs630923
ebirs630923
HLIrs630923
Exacrs630923
Varsomers630923
Maprs630923
PheGenIrs630923
hapmaprs630923
1000 genomesrs630923
hgdprs630923
ensemblrs630923
gopubmedrs630923
geneviewrs630923
scholarrs630923
googlers630923
pharmgkbrs630923
gwascentralrs630923
openSNPrs630923
23andMers630923
23andMe allrs630923
SNP Nexus

SNPshotrs630923
SNPdbers630923
MSV3drs630923
GWAS Ctlgrs630923
GMAF0.1065
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21833088OA-icon.png]
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 23128233OA-icon.png]
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 23250934OA-icon.png] Serum levels of the chemokine CXCL13, genetic variation in CXCL13 and its receptor CXCR5, and HIV-associated non-hodgkin B-cell lymphoma risk


[PMID 23739915OA-icon.png] MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis