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rs859637

From SNPedia

Orientationminus
Stabilizedminus
Make rs859637(A;A)
Make rs859637(A;G)
Make rs859637(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position172741860
is asnp
is mentioned by
dbSNPrs859637
ebirs859637
HLIrs859637
Exacrs859637
Varsomers859637
Maprs859637
PheGenIrs859637
hapmaprs859637
1000 genomesrs859637
hgdprs859637
ensemblrs859637
gopubmedrs859637
geneviewrs859637
scholarrs859637
googlers859637
pharmgkbrs859637
gwascentralrs859637
openSNPrs859637
23andMers859637
23andMe allrs859637
SNP Nexus

SNPshotrs859637
SNPdbers859637
MSV3drs859637
GWAS Ctlgrs859637
GMAF0.4394
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20190752OA-icon.png]
Trait Celiac disease
Title Multiple common variants for celiac disease influencing immune gene expression
Risk Allele A
P-val 0.000002
Odds Ratio 1.10 [1.06-1.14]