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rs4959053

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 3 Increased (>4.4x?) risk of Behcet's disease
(A;G) 2 Increased (4.38x) risk of Behcet's disease
(G;G) 0 Normal
ReferenceGRCh38 38.1/141
Chromosome6
Position31131800
GenePSORS1C1
is asnp
is mentioned by
dbSNPrs4959053
dbSNP (classic)rs4959053
ClinGenrs4959053
ebirs4959053
HLIrs4959053
Exacrs4959053
Gnomadrs4959053
Varsomers4959053
LitVarrs4959053
Maprs4959053
PheGenIrs4959053
Biobankrs4959053
1000 genomesrs4959053
hgdprs4959053
ensemblrs4959053
geneviewrs4959053
scholarrs4959053
googlers4959053
pharmgkbrs4959053
gwascentralrs4959053
openSNPrs4959053
23andMers4959053
SNPshotrs4959053
SNPdbers4959053
MSV3drs4959053
GWAS Ctlgrs4959053
GMAF0.0652
Max Magnitude3

[PMID 23001997] A 2012 study of ~600 Chinese patients with Behcet's disease indicated an association with rs4959053; the odds ratio was 4.38 (CI: 3.2-5.9, p = 2.2e-20). This SNP, one of several found in one of three linkage blocks in the region showing association with Behcet's disease, showed the strongest association.

? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23001997]
Trait Behcet's disease
Title Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study.
Risk Allele
P-val 2E-20
Odds Ratio 4.38 [3.20-5.99]