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rs10495903

From SNPedia

Orientationplus
Stabilizedplus
Make rs10495903(C;C)
Make rs10495903(C;T)
Make rs10495903(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position43579779
GeneTHADA
is asnp
is mentioned by
dbSNPrs10495903
ebirs10495903
HLIrs10495903
Exacrs10495903
Varsomers10495903
Maprs10495903
PheGenIrs10495903
hapmaprs10495903
1000 genomesrs10495903
hgdprs10495903
ensemblrs10495903
gopubmedrs10495903
geneviewrs10495903
scholarrs10495903
googlers10495903
pharmgkbrs10495903
gwascentralrs10495903
openSNPrs10495903
23andMers10495903
23andMe allrs10495903
SNP Nexus

SNPshotrs10495903
SNPdbers10495903
MSV3drs10495903
GWAS Ctlgrs10495903
GMAF0.0955
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21102463OA-icon.png]
Trait
Title Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Risk Allele T
P-val 2E-14
Odds Ratio 1.1400 [1.09-1.20]
GWAS snp
PMID [PMID 23128233OA-icon.png]
Trait Inflammatory bowel disease
Title Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele T
P-val 8E-12
Odds Ratio 1.09 [1.041-1.131]