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rs6503695

From SNPedia

Orientationplus
Stabilizedplus
Make rs6503695(C;C)
Make rs6503695(C;T)
Make rs6503695(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position42347515
GeneSTAT3
is asnp
is mentioned by
dbSNPrs6503695
ebirs6503695
HLIrs6503695
Exacrs6503695
Varsomers6503695
Maprs6503695
PheGenIrs6503695
hapmaprs6503695
1000 genomesrs6503695
hgdprs6503695
ensemblrs6503695
gopubmedrs6503695
geneviewrs6503695
scholarrs6503695
googlers6503695
pharmgkbrs6503695
gwascentralrs6503695
openSNPrs6503695
23andMers6503695
23andMe allrs6503695
SNP Nexus

SNPshotrs6503695
SNPdbers6503695
MSV3drs6503695
GWAS Ctlgrs6503695
GMAF0.3315
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 22205606] JAK2 and STAT3 polymorphisms in a Han Chinese Population with Behcet's disease

[PMID 17636079OA-icon.png] Common STAT3 variants are not associated with obesity or insulin resistance in female twins.

[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 20065083OA-icon.png] A polymorphism associated with STAT3 expression and response of chronic myeloid leukemia to interferon alpha.

[PMID 20159113OA-icon.png] Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.

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


[PMID 23611997] JAK1, but not JAK2 and STAT3, confers susceptibility to Vogt-Koyanagi-Harada (VKH) syndrome in a Han Chinese population