Have questions? Visit https://www.reddit.com/r/SNPedia

rs1456896

From SNPedia

Orientationminus
Stabilizedminus
Make rs1456896(A;A)
Make rs1456896(A;G)
Make rs1456896(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position50264865
is asnp
is mentioned by
dbSNPrs1456896
ebirs1456896
HLIrs1456896
Exacrs1456896
Varsomers1456896
Maprs1456896
PheGenIrs1456896
hapmaprs1456896
1000 genomesrs1456896
hgdprs1456896
ensemblrs1456896
gopubmedrs1456896
geneviewrs1456896
scholarrs1456896
googlers1456896
pharmgkbrs1456896
gwascentralrs1456896
openSNPrs1456896
23andMers1456896
23andMe allrs1456896
SNP Nexus

SNPshotrs1456896
SNPdbers1456896
MSV3drs1456896
GWAS Ctlgrs1456896
GMAF0.4008
Max Magnitude
? (A;A) (A;G) (G;G) 28
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 7E-15
Odds Ratio 1.09 [1.055-1.123]
GWAS snp
PMID [PMID 21102463OA-icon.png]
Trait Crohn's disease
Title Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.
Risk Allele T
P-val 1E-8
Odds Ratio 1.14 [1.09-1.20]