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

rs7574070

From SNPedia

Orientationplus
Stabilizedplus
Make rs7574070(A;A)
Make rs7574070(A;C)
Make rs7574070(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position191145762
GeneSTAT4
is asnp
is mentioned by
dbSNPrs7574070
ebirs7574070
HLIrs7574070
Exacrs7574070
Varsomers7574070
Maprs7574070
PheGenIrs7574070
hapmaprs7574070
1000 genomesrs7574070
hgdprs7574070
ensemblrs7574070
gopubmedrs7574070
geneviewrs7574070
scholarrs7574070
googlers7574070
pharmgkbrs7574070
gwascentralrs7574070
openSNPrs7574070
23andMers7574070
23andMe allrs7574070
SNP Nexus

SNPshotrs7574070
SNPdbers7574070
MSV3drs7574070
GWAS Ctlgrs7574070
GMAF0.4839
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 23001997] Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study

GWAS snp
PMID [PMID 23291587OA-icon.png]
Trait Behcet's disease
Title Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.
Risk Allele A
P-val 1E-9
Odds Ratio 1.27 [1.17-1.37]