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rs878860

From SNPedia

Orientationplus
Stabilizedplus
Make rs878860(C;C)
Make rs878860(C;T)
Make rs878860(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position7946812
is asnp
is mentioned by
dbSNPrs878860
dbSNP (classic)rs878860
ClinGenrs878860
ebirs878860
HLIrs878860
Exacrs878860
Gnomadrs878860
Varsomers878860
LitVarrs878860
Maprs878860
PheGenIrs878860
Biobankrs878860
1000 genomesrs878860
hgdprs878860
ensemblrs878860
geneviewrs878860
scholarrs878860
googlers878860
pharmgkbrs878860
gwascentralrs878860
openSNPrs878860
23andMers878860
SNPshotrs878860
SNPdbers878860
MSV3drs878860
GWAS Ctlgrs878860
GMAF0.371
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23042114]
Trait Atopic dermatitis
Title Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population.
Risk Allele G
P-val 2E-22
Odds Ratio 1.31 [1.24-1.38]