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rs1958589

From SNPedia

Orientationplus
Stabilizedplus
Make rs1958589(C;C)
Make rs1958589(C;T)
Make rs1958589(T;T)
ReferenceGRCh38 38.1/142
Chromosome14
Position34375170
is asnp
is mentioned by
dbSNPrs1958589
ebirs1958589
HLIrs1958589
Exacrs1958589
Varsomers1958589
Maprs1958589
PheGenIrs1958589
hapmaprs1958589
1000 genomesrs1958589
hgdprs1958589
ensemblrs1958589
gopubmedrs1958589
geneviewrs1958589
scholarrs1958589
googlers1958589
pharmgkbrs1958589
gwascentralrs1958589
openSNPrs1958589
23andMers1958589
23andMe allrs1958589
SNP Nexus

SNPshotrs1958589
SNPdbers1958589
MSV3drs1958589
GWAS Ctlgrs1958589
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 4E-6
Odds Ratio NR NR