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rs16887812

From SNPedia

Orientationplus
Stabilizedplus
Make rs16887812(C;C)
Make rs16887812(C;T)
Make rs16887812(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position56345966
is asnp
is mentioned by
dbSNPrs16887812
ebirs16887812
HLIrs16887812
Exacrs16887812
Varsomers16887812
Maprs16887812
PheGenIrs16887812
hapmaprs16887812
1000 genomesrs16887812
hgdprs16887812
ensemblrs16887812
gopubmedrs16887812
geneviewrs16887812
scholarrs16887812
googlers16887812
pharmgkbrs16887812
gwascentralrs16887812
openSNPrs16887812
23andMers16887812
23andMe allrs16887812
SNP Nexus

SNPshotrs16887812
SNPdbers16887812
MSV3drs16887812
GWAS Ctlgrs16887812
GMAF0.303
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 7E-6
Odds Ratio 1.10 [1.05-1.14]