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rs9550642

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 2.2x risk
(A;G) 1.3x risk
(G;G) 0 normal
ReferenceGRCh38 38.1/141
Chromosome13
Position20375953
GeneLOC100133618
is asnp
is mentioned by
dbSNPrs9550642
ebirs9550642
HLIrs9550642
Exacrs9550642
Varsomers9550642
Maprs9550642
PheGenIrs9550642
hapmaprs9550642
1000 genomesrs9550642
hgdprs9550642
ensemblrs9550642
gopubmedrs9550642
geneviewrs9550642
scholarrs9550642
googlers9550642
pharmgkbrs9550642
gwascentralrs9550642
openSNPrs9550642
23andMers9550642
23andMe allrs9550642
SNP Nexus

SNPshotrs9550642
SNPdbers9550642
MSV3drs9550642
GWAS Ctlgrs9550642
GMAF0.1368
Max Magnitude0
? (A;A) (A;G) (G;G) 28
rs9550642 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 1.34 (CI 1.15-1.56), and for homozygotes, 2.23 (CI 1.21-4.13). [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.