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rs11162922

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 2x risk
(A;G) 1.3x risk
(G;G) normal
ReferenceGRCh38 38.1/141
Chromosome1
Position80106373
is asnp
is mentioned by
dbSNPrs11162922
ebirs11162922
HLIrs11162922
Exacrs11162922
Varsomers11162922
Maprs11162922
PheGenIrs11162922
hapmaprs11162922
1000 genomesrs11162922
hgdprs11162922
ensemblrs11162922
gopubmedrs11162922
geneviewrs11162922
scholarrs11162922
googlers11162922
pharmgkbrs11162922
gwascentralrs11162922
openSNPrs11162922
23andMers11162922
23andMe allrs11162922
SNP Nexus

SNPshotrs11162922
SNPdbers11162922
MSV3drs11162922
GWAS Ctlgrs11162922
GMAF0.1938
Max Magnitude
? (A;A) (A;G) (G;G) 28
rs11162922 has been reported in a large study to be associated with rheumatoid arthritis.

The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with heterozygotes is 1.27 (CI 0.41-4.01), and for homozygotes, 2.00 (CI 0.64-6.20). [PMID 17554300OA-icon.png]


[PMID 18794857OA-icon.png] Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13.


[PMID 20017963OA-icon.png] Representation of genetic association via attributable familial relative risks in order to identify polymorphisms functionally relevant to rheumatoid arthritis.