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rs593982

From SNPedia

Orientationminus
Stabilizedminus
Make rs593982(A;A)
Make rs593982(A;G)
Make rs593982(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position65745636
is asnp
is mentioned by
dbSNPrs593982
dbSNP (classic)rs593982
ClinGenrs593982
ebirs593982
HLIrs593982
Exacrs593982
Gnomadrs593982
Varsomers593982
LitVarrs593982
Maprs593982
PheGenIrs593982
Biobankrs593982
1000 genomesrs593982
hgdprs593982
ensemblrs593982
geneviewrs593982
scholarrs593982
googlers593982
pharmgkbrs593982
gwascentralrs593982
openSNPrs593982
23andMers593982
SNPshotrs593982
SNPdbers593982
MSV3drs593982
GWAS Ctlgrs593982
GMAF0.2759
Max Magnitude0
? (A;A) (A;G) (G;G) 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 C
P-val 6E-7
Odds Ratio 1.23 [NR]