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rs10886159

From SNPedia

Orientationplus
Stabilizedplus
Make rs10886159(C;C)
Make rs10886159(C;T)
Make rs10886159(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position117854099
is asnp
is mentioned by
dbSNPrs10886159
ebirs10886159
HLIrs10886159
Exacrs10886159
Varsomers10886159
Maprs10886159
PheGenIrs10886159
hapmaprs10886159
1000 genomesrs10886159
hgdprs10886159
ensemblrs10886159
gopubmedrs10886159
geneviewrs10886159
scholarrs10886159
googlers10886159
pharmgkbrs10886159
gwascentralrs10886159
openSNPrs10886159
23andMers10886159
23andMe allrs10886159
SNP Nexus

SNPshotrs10886159
SNPdbers10886159
MSV3drs10886159
GWAS Ctlgrs10886159
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 7E-7
Odds Ratio NR NR