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rs4911642

From SNPedia

Orientationminus
Stabilizedplus
Make rs4911642(C;C)
Make rs4911642(C;T)
Make rs4911642(T;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position15473564
is asnp
is mentioned by
dbSNPrs4911642
ebirs4911642
HLIrs4911642
Exacrs4911642
Varsomers4911642
Maprs4911642
PheGenIrs4911642
hapmaprs4911642
1000 genomesrs4911642
hgdprs4911642
ensemblrs4911642
gopubmedrs4911642
geneviewrs4911642
scholarrs4911642
googlers4911642
pharmgkbrs4911642
gwascentralrs4911642
openSNPrs4911642
23andMers4911642
23andMe allrs4911642
SNP Nexus

SNPshotrs4911642
SNPdbers4911642
MSV3drs4911642
GWAS Ctlgrs4911642
Max Magnitude
GWAS snp
PMID [PMID 23936387OA-icon.png]
Trait Celiac disease
Title A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.
Risk Allele C
P-val 5E-6
Odds Ratio NR NR