rs9266406

plus

Geno	Mag	Summary
(A;A)	2	Slightly increased (>2.3x) risk for Behcet's disease
(A;G)	2	Slightly increased risk for Behcet's disease
(G;G)	0	common/normal

Reference

GRCh38 38.1/141

Chromosome

6

Position

31368641

Gene

DHFRP2

is a	snp
is	mentioned by
dbSNP	rs9266406
dbSNP (classic)	rs9266406
ClinGen	rs9266406
ebi	rs9266406
HLI	rs9266406
Exac	rs9266406
Gnomad	rs9266406
Varsome	rs9266406
LitVar	rs9266406
Map	rs9266406
PheGenI	rs9266406
Biobank	rs9266406
1000 genomes	rs9266406
hgdp	rs9266406
ensembl	rs9266406
geneview	rs9266406
scholar	rs9266406
google	rs9266406
pharmgkb	rs9266406
gwascentral	rs9266406
openSNP	rs9266406
23andMe	rs9266406
SNPshot	rs9266406
SNPdbe	rs9266406
MSV3d	rs9266406
GWAS Ctlg	rs9266406

GMAF

0.2617

Max Magnitude

2

[PMID 23001997] A 2012 study of ~600 Chinese patients with Behcet's disease indicated an association with rs9266406(A); the odds ratio was 2.3 (CI: 1.7-2.9, p = 1.9e-10). This SNP was one of several found in one of three linkage blocks in the region showing association with Behcet's disease; the strongest association was for rs4959053, found in one of the other linkage blocks.

?

(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-10
Odds Ratio	2.29 [1.77-2.95]