rs6601764

plus

Geno	Mag	Summary
(C;C)	2	1.52x increased risk of developing Crohn's disease
(C;T)	1.5	1.16x increased risk of developing Crohn's disease
(T;T)	1	Normal risk of developing Crohn's disease

Reference

GRCh38 38.1/142

Chromosome

10

Position

3820350

is a	snp
is	mentioned by
dbSNP	rs6601764
dbSNP (classic)	rs6601764
ClinGen	rs6601764
ebi	rs6601764
HLI	rs6601764
Exac	rs6601764
Gnomad	rs6601764
Varsome	rs6601764
LitVar	rs6601764
Map	rs6601764
PheGenI	rs6601764
Biobank	rs6601764
1000 genomes	rs6601764
hgdp	rs6601764
ensembl	rs6601764
geneview	rs6601764
scholar	rs6601764
google	rs6601764
pharmgkb	rs6601764
gwascentral	rs6601764
openSNP	rs6601764
23andMe	rs6601764
SNPshot	rs6601764
SNPdbe	rs6601764
MSV3d	rs6601764
GWAS Ctlg	rs6601764

GMAF

0.3669

Max Magnitude

2

?

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

28

rs6601764 has been reported in a large study to be associated with Crohn's disease.

The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 1.16 (CI 1.01-1.33), and for homozygotes, 1.52 (CI 1.28-1.80). [PMID 17554300 ]