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rs1467199

From SNPedia

Orientationplus
Stabilizedplus
Make rs1467199(C;C)
Make rs1467199(C;G)
Make rs1467199(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position191015776
GeneSTAT1
is asnp
is mentioned by
dbSNPrs1467199
ebirs1467199
HLIrs1467199
Exacrs1467199
Varsomers1467199
Maprs1467199
PheGenIrs1467199
hapmaprs1467199
1000 genomesrs1467199
hgdprs1467199
ensemblrs1467199
gopubmedrs1467199
geneviewrs1467199
scholarrs1467199
googlers1467199
pharmgkbrs1467199
gwascentralrs1467199
openSNPrs1467199
23andMers1467199
23andMe allrs1467199
SNP Nexus

SNPshotrs1467199
SNPdbers1467199
MSV3drs1467199
GWAS Ctlgrs1467199
GMAF0.3352
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 19644876] Association of STAT4 and BLK, but not BANK1 or IRF5, with primary antiphospholipid syndrome

[PMID 17932559OA-icon.png] Association of STAT4 with rheumatoid arthritis in the Korean population.

[PMID 18520591OA-icon.png] Sequence variants in host cell factor C1 are associated with Meniere's disease.

[PMID 19019891OA-icon.png] STAT4 associates with systemic lupus erythematosus through two independent effects that correlate with gene expression and act additively with IRF5 to increase risk.

[PMID 19753122OA-icon.png] Analysis of SNPs and haplotypes in vitamin D pathway genes and renal cancer risk.


[PMID 25707685] STAT1 single nucleotide polymorphisms and susceptibility to immune thrombocytopenia