rs9348876

plus

Geno	Mag	Summary
(C;C)	0

Make rs9348876(C;T)

Make rs9348876(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31607499

is a	snp
is	mentioned by
dbSNP	rs9348876
dbSNP (classic)	rs9348876
ClinGen	rs9348876
ebi	rs9348876
HLI	rs9348876
Exac	rs9348876
Gnomad	rs9348876
Varsome	rs9348876
LitVar	rs9348876
Map	rs9348876
PheGenI	rs9348876
Biobank	rs9348876
1000 genomes	rs9348876
hgdp	rs9348876
ensembl	rs9348876
geneview	rs9348876
scholar	rs9348876
google	rs9348876
pharmgkb	rs9348876
gwascentral	rs9348876
openSNP	rs9348876
23andMe	rs9348876
SNPshot	rs9348876
SNPdbe	rs9348876
MSV3d	rs9348876
GWAS Ctlg	rs9348876

GMAF

0.1107

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

GWAS snp
PMID	[PMID 22936669]
Trait	Crohn's disease
Title	A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.
Risk Allele	T
P-val	3E-6
Odds Ratio	1.41 [1.22-1.63]

[PMID 20064070 ] Multistage genomewide association study identifies a locus at 1q41 associated with rate of HIV-1 disease progression to clinical AIDS.