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rs4899260

From SNPedia

Orientationplus
Stabilizedplus
Make rs4899260(C;C)
Make rs4899260(C;T)
Make rs4899260(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position68811487
is asnp
is mentioned by
dbSNPrs4899260
ebirs4899260
HLIrs4899260
Exacrs4899260
Varsomers4899260
Maprs4899260
PheGenIrs4899260
hapmaprs4899260
1000 genomesrs4899260
hgdprs4899260
ensemblrs4899260
gopubmedrs4899260
geneviewrs4899260
scholarrs4899260
googlers4899260
pharmgkbrs4899260
gwascentralrs4899260
openSNPrs4899260
23andMers4899260
23andMe allrs4899260
SNP Nexus

SNPshotrs4899260
SNPdbers4899260
MSV3drs4899260
GWAS Ctlgrs4899260
GMAF0.1988
Max Magnitude
? (C;C) (C;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 A
P-val 4E-7
Odds Ratio 1.12 [1.07-1.16]