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rs11122895

From SNPedia

Orientationplus
Stabilizedplus
Make rs11122895(C;C)
Make rs11122895(C;T)
Make rs11122895(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position111712578
is asnp
is mentioned by
dbSNPrs11122895
ebirs11122895
HLIrs11122895
Exacrs11122895
Varsomers11122895
Maprs11122895
PheGenIrs11122895
hapmaprs11122895
1000 genomesrs11122895
hgdprs11122895
ensemblrs11122895
gopubmedrs11122895
geneviewrs11122895
scholarrs11122895
googlers11122895
pharmgkbrs11122895
gwascentralrs11122895
openSNPrs11122895
23andMers11122895
23andMe allrs11122895
SNP Nexus

SNPshotrs11122895
SNPdbers11122895
MSV3drs11122895
GWAS Ctlgrs11122895
GMAF0.2521
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23817571]
Trait Allergic sensitization
Title Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization.
Risk Allele T
P-val 2E-6
Odds Ratio 1.09 [1.05-1.13]