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rs11676922

From SNPedia

Orientationplus
Stabilizedplus
Make rs11676922(A;A)
Make rs11676922(A;T)
Make rs11676922(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position100190478
is asnp
is mentioned by
dbSNPrs11676922
ebirs11676922
HLIrs11676922
Exacrs11676922
Varsomers11676922
Maprs11676922
PheGenIrs11676922
hapmaprs11676922
1000 genomesrs11676922
hgdprs11676922
ensemblrs11676922
gopubmedrs11676922
geneviewrs11676922
scholarrs11676922
googlers11676922
pharmgkbrs11676922
gwascentralrs11676922
openSNPrs11676922
23andMers11676922
23andMe allrs11676922
SNP Nexus

SNPshotrs11676922
SNPdbers11676922
MSV3drs11676922
GWAS Ctlgrs11676922
GMAF0.4922
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 20453842OA-icon.png]
Trait Rheumatoid arthritis
Title Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk lock
Risk Allele T
P-val 1E-14
Odds Ratio 1.12 [NR]
GWAS snp
PMID [PMID 24782177]
Trait Rheumatoid arthritis
Title Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans.
Risk Allele T
P-val 2E-8
Odds Ratio 1.13 [NR]