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rs13128441

From SNPedia

Orientationplus
Stabilizedplus
Make rs13128441(C;C)
Make rs13128441(C;T)
Make rs13128441(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position5160662
GeneSTK32B
is asnp
is mentioned by
dbSNPrs13128441
ebirs13128441
HLIrs13128441
Exacrs13128441
Varsomers13128441
Maprs13128441
PheGenIrs13128441
hapmaprs13128441
1000 genomesrs13128441
hgdprs13128441
ensemblrs13128441
gopubmedrs13128441
geneviewrs13128441
scholarrs13128441
googlers13128441
pharmgkbrs13128441
gwascentralrs13128441
openSNPrs13128441
23andMers13128441
23andMe allrs13128441
SNP Nexus

SNPshotrs13128441
SNPdbers13128441
MSV3drs13128441
GWAS Ctlgrs13128441
Max Magnitude
? (C;C) (C;T) (T;T) 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 C
P-val 8E-6
Odds Ratio NR NR