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

rs9891119

From SNPedia

Orientationplus
Stabilizedplus
Make rs9891119(A;A)
Make rs9891119(A;C)
Make rs9891119(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position42355962
GeneSTAT3
is asnp
is mentioned by
dbSNPrs9891119
ebirs9891119
HLIrs9891119
Exacrs9891119
Varsomers9891119
Maprs9891119
PheGenIrs9891119
hapmaprs9891119
1000 genomesrs9891119
hgdprs9891119
ensemblrs9891119
gopubmedrs9891119
geneviewrs9891119
scholarrs9891119
googlers9891119
pharmgkbrs9891119
gwascentralrs9891119
openSNPrs9891119
23andMers9891119
23andMe allrs9891119
SNP Nexus

SNPshotrs9891119
SNPdbers9891119
MSV3drs9891119
GWAS Ctlgrs9891119
GMAF0.3714
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23266558]
Trait Crohn's disease
Title A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population.
Risk Allele A
P-val 2E-15
Odds Ratio 1.37 [1.27-1.48]
GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait Multiple sclerosis
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele C
P-val 2E-10
Odds Ratio 1.11 [1.09-1.12]


[PMID 18451776] Study of genetic variation in the STAT3 on obesity and insulin resistance in male adults.


[PMID 18789715] Genetic variants in STAT3 are associated with nonalcoholic fatty liver disease.


[PMID 21310444] Mitochondrial DNA copy number is modulated by genetic variation in the signal transducer and activator of transcription 3 (STAT3).