rs12567232

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	2	Increased risk for Crohn's Disease
(A;G)	2	Increased risk for Crohn's Disease
(G;G)	0	normal

Reference

GRCh38 38.1/141

Chromosome

1

Position

67262335

is a	snp
is	mentioned by
dbSNP	rs12567232
dbSNP (classic)	rs12567232
ClinGen	rs12567232
ebi	rs12567232
HLI	rs12567232
Exac	rs12567232
Gnomad	rs12567232
Varsome	rs12567232
LitVar	rs12567232
Map	rs12567232
PheGenI	rs12567232
Biobank	rs12567232
1000 genomes	rs12567232
hgdp	rs12567232
ensembl	rs12567232
geneview	rs12567232
scholar	rs12567232
google	rs12567232
pharmgkb	rs12567232
gwascentral	rs12567232
openSNP	rs12567232
23andMe	rs12567232
SNPshot	rs12567232
SNPdbe	rs12567232
MSV3d	rs12567232
GWAS Ctlg	rs12567232

GMAF

0.3632

Max Magnitude

2

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

GWAS
SNP	rs12567232
PubMedID	[PMID 17804789]
Condition	Crohn's disease
Gene	IL23R
Risk Allele	A
pValue	1.00E-008
OR	1.38
95% CI	1.23-1.53