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rs10439884

From SNPedia

Orientationminus
Stabilizedplus
Make rs10439884(A;A)
Make rs10439884(A;G)
Make rs10439884(G;G)
ReferenceGRCh38 38.1/142
Chromosome21
Position10540506
GeneTPTE
is asnp
is mentioned by
dbSNPrs10439884
ebirs10439884
HLIrs10439884
Exacrs10439884
Varsomers10439884
Maprs10439884
PheGenIrs10439884
hapmaprs10439884
1000 genomesrs10439884
hgdprs10439884
ensemblrs10439884
gopubmedrs10439884
geneviewrs10439884
scholarrs10439884
googlers10439884
pharmgkbrs10439884
gwascentralrs10439884
openSNPrs10439884
23andMers10439884
23andMe allrs10439884
SNP Nexus

SNPshotrs10439884
SNPdbers10439884
MSV3drs10439884
GWAS Ctlgrs10439884
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 A
P-val 2E-6
Odds Ratio NR NR