rs925847

Orientation

plus

Stabilized

plus

Make rs925847(C;C)

Make rs925847(C;T)

Make rs925847(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

191032814

Gene	LOC105373805, STAT4

is a	snp
is	mentioned by
dbSNP	rs925847
dbSNP (classic)	rs925847
ClinGen	rs925847
ebi	rs925847
HLI	rs925847
Exac	rs925847
Gnomad	rs925847
Varsome	rs925847
LitVar	rs925847
Map	rs925847
PheGenI	rs925847
Biobank	rs925847
1000 genomes	rs925847
hgdp	rs925847
ensembl	rs925847
geneview	rs925847
scholar	rs925847
google	rs925847
pharmgkb	rs925847
gwascentral	rs925847
openSNP	rs925847
23andMe	rs925847
SNPshot	rs925847
SNPdbe	rs925847
MSV3d	rs925847
GWAS Ctlg	rs925847

GMAF

0.3659

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 20176035] Association of signal transducer and activator of transcription 4 genetic variants with extra-intestinal manifestations in inflammatory bowel disease

[PMID 14681825] Mutation of CERKL, a novel human ceramide kinase gene, causes autosomal recessive retinitis pigmentosa (RP26).

[PMID 17932559] Association of STAT4 with rheumatoid arthritis in the Korean population.

[PMID 18579578] A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of IRF5.

[PMID 18803832] Role of STAT4 polymorphisms in systemic lupus erythematosus in a Japanese population: a case-control association study of the STAT1-STAT4 region.

[PMID 19282076] Association of single-nucleotide polymorphisms in JAK3, STAT4, and STAT6 with new cardiovascular events in incident dialysis patients.

[PMID 20454450] Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.

[PMID 22569826] Abnormal Genetic and Epigenetic Changes in Signal Transducer and Activator of Transcription 4 in the Pathogenesis of Inflammatory Bowel Diseases.

[PMID 32973967] SNPs in the interleukin-12 signaling pathway are associated with breast cancer risk in Puerto Rican women.