rs1793004

minus

Geno	Mag	Summary
(C;C)		increased risk for Crohn's disease
(C;G)		?
(G;G)		0.89x decreased risk for Crohn's disease

Reference

GRCh38 38.1/141

Chromosome

11

Position

20677383

Gene

NELL1

is a	snp
is	mentioned by
dbSNP	rs1793004
dbSNP (classic)	rs1793004
ClinGen	rs1793004
ebi	rs1793004
HLI	rs1793004
Exac	rs1793004
Gnomad	rs1793004
Varsome	rs1793004
LitVar	rs1793004
Map	rs1793004
PheGenI	rs1793004
Biobank	rs1793004
1000 genomes	rs1793004
hgdp	rs1793004
ensembl	rs1793004
geneview	rs1793004
scholar	rs1793004
google	rs1793004
pharmgkb	rs1793004
gwascentral	rs1793004
openSNP	rs1793004
23andMe	rs1793004
SNPshot	rs1793004
SNPdbe	rs1793004
MSV3d	rs1793004
GWAS Ctlg	rs1793004

GMAF

0.3512

Max Magnitude

0

?

(C;C) (C;G) (G;G)

28

rs1793004 is a SNP in the NELL1 gene that was found in a genome-wide association study to be associated with Crohn's disease.

In several European populations, the most common allele, rs1793004(C), was associated with increased risk for Crohn's disease. Conversely, the odds ratio (pooled over several populations) for the minor allele, rs1793004(G), was 0.89 (CI: 0.69-1.14, p=0.0037).[PMID 17684544 ]

GWAS
SNP	rs1793004
PubMedID	[PMID 17684544 ]
Condition	Irritable bowel syndrome
Gene	NELL1
Risk Allele
pValue	3.00E-006
OR	1.3
95% CI	1.12-1.52