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rs2074404

From SNPedia

Orientationplus
Stabilizedplus
Make rs2074404(G;G)
Make rs2074404(G;T)
Make rs2074404(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position46788073
GeneWNT3
is asnp
is mentioned by
dbSNPrs2074404
ebirs2074404
HLIrs2074404
Exacrs2074404
Varsomers2074404
Maprs2074404
PheGenIrs2074404
hapmaprs2074404
1000 genomesrs2074404
hgdprs2074404
ensemblrs2074404
gopubmedrs2074404
geneviewrs2074404
scholarrs2074404
googlers2074404
pharmgkbrs2074404
gwascentralrs2074404
openSNPrs2074404
23andMers2074404
23andMe allrs2074404
SNP Nexus

SNPshotrs2074404
SNPdbers2074404
MSV3drs2074404
GWAS Ctlgrs2074404
GMAF0.348
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 20190752OA-icon.png]
Trait Celiac disease
Title Multiple common variants for celiac disease influencing immune gene expression
Risk Allele
P-val 0.000001
Odds Ratio 1.11 [1.06-1.16]


[PMID 24871462] Coeliac disease-associated polymorphisms influence thymic gene expression