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rs4930144

From SNPedia

Orientationplus
Stabilizedplus
Make rs4930144(A;A)
Make rs4930144(A;G)
Make rs4930144(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2027258
is asnp
is mentioned by
dbSNPrs4930144
ebirs4930144
HLIrs4930144
Exacrs4930144
Varsomers4930144
Maprs4930144
PheGenIrs4930144
hapmaprs4930144
1000 genomesrs4930144
hgdprs4930144
ensemblrs4930144
gopubmedrs4930144
geneviewrs4930144
scholarrs4930144
googlers4930144
pharmgkbrs4930144
gwascentralrs4930144
openSNPrs4930144
23andMers4930144
23andMe allrs4930144
SNP Nexus

SNPshotrs4930144
SNPdbers4930144
MSV3drs4930144
GWAS Ctlgrs4930144
Max Magnitude
? (A;A) (A;G) (G;G) 28
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 A
P-val 7E-6
Odds Ratio NR NR