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rs3024866

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3024866(C;T)
Make rs3024866(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position191058115
GeneSTAT4
is asnp
is mentioned by
dbSNPrs3024866
dbSNP (classic)rs3024866
ClinGenrs3024866
ebirs3024866
HLIrs3024866
Exacrs3024866
Gnomadrs3024866
Varsomers3024866
LitVarrs3024866
Maprs3024866
PheGenIrs3024866
Biobankrs3024866
1000 genomesrs3024866
hgdprs3024866
ensemblrs3024866
geneviewrs3024866
scholarrs3024866
googlers3024866
pharmgkbrs3024866
gwascentralrs3024866
openSNPrs3024866
23andMers3024866
SNPshotrs3024866
SNPdbers3024866
MSV3drs3024866
GWAS Ctlgrs3024866
GMAF0.4642
Max Magnitude0
? (C;C) (C;T) (T;T) 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 18579578OA-icon.png] 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 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 23360093] Association study of STAT4 polymorphisms and type 1 diabetes in Northeastern Chinese Han population


ClinVar
Risk rs3024866(T;T)
Alt rs3024866(T;T)
Reference Rs3024866(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene STAT4
CLNDBN not specified
Reversed 1
HGVS NC_000002.11:g.191922841G>A
CLNSRC
CLNACC RCV000455357.1,