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rs17616434

From SNPedia

Orientationplus
Stabilizedplus
Make rs17616434(C;C)
Make rs17616434(C;T)
Make rs17616434(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position38811255
is asnp
is mentioned by
dbSNPrs17616434
dbSNP (classic)rs17616434
ClinGenrs17616434
ebirs17616434
HLIrs17616434
Exacrs17616434
Gnomadrs17616434
Varsomers17616434
LitVarrs17616434
Maprs17616434
PheGenIrs17616434
Biobankrs17616434
1000 genomesrs17616434
hgdprs17616434
ensemblrs17616434
geneviewrs17616434
scholarrs17616434
googlers17616434
pharmgkbrs17616434
gwascentralrs17616434
openSNPrs17616434
23andMers17616434
SNPshotrs17616434
SNPdbers17616434
MSV3drs17616434
GWAS Ctlgrs17616434
GMAF0.4656
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23817571OA-icon.png]
Trait Allergic sensitization
Title Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization.
Risk Allele T
P-val 5E-11
Odds Ratio 1.23 [1.18-1.29]