Rs11761231

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is asnp
is mentioned by
dbSNPrs11761231
hapmaprs11761231
hgdprs11761231
ensemblrs11761231
gopubmedrs11761231
scholarrs11761231
googlers11761231
pharmgkbrs11761231
hgvbaseg2prs11761231
medrefsnprs11761231
23andMers11761231
SNP Nexus

Chromosome7
Orientationplus
Position131020579
GenotypeEffect
rs11761231(C;C)
rs11761231(C;T)
rs11761231(T;T)normal


Genotypes Magnitude Summary
Rs11761231(A;A) 00
Rs11761231(C;C)
Rs11761231(C;T)
Rs11761231(T;T) 00 normal
rs11761231 has been reported in a large study to be associated with rheumatoid arthritis, particularly in females.

The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 1.44 (CI 1.19-1.75), and for homozygotes, 1.64 (CI 1.35-1.99). [PMID 17554300]

[PMID 19116934] The association between rs11761231 and rheumatoid arthritis did not reproduce in a North American population, emphasizing "the need to carefully account for population structure to avoid false-positive disease associations".

? (C;C) (C;T) (T;T)
GWAS
SNP rs11761231
PubMedID [PMID 17554300]
Condition Rheumatoid arthritis
Gene Intergenic
Risk Allele C
pValue 4.00E-007
OR 1.32
95% CI


PharmGKBPA162356639
Name
AnnotationGWAS Results: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (Initial Sample Size: 1,860 cases, 2,938 controls; Replication Sample Size: NR; Risk Allele: rs11761231-C). This variant is associated with rheumatoid arthritis.
Gene-
Featue
EvidencePubMed ID:17554300; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesArthritis, Rheumatoid
Curation LevelNon-Curated