rs7807268
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 2 | 1.4x risk for Crohn's disease |
(C;G) | 2 | 1.3x risk for Crohn's disease |
(G;G) | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 148560956 |
is a | snp |
is | mentioned by |
dbSNP | rs7807268 |
dbSNP (classic) | rs7807268 |
ClinGen | rs7807268 |
ebi | rs7807268 |
HLI | rs7807268 |
Exac | rs7807268 |
Gnomad | rs7807268 |
Varsome | rs7807268 |
LitVar | rs7807268 |
Map | rs7807268 |
PheGenI | rs7807268 |
Biobank | rs7807268 |
1000 genomes | rs7807268 |
hgdp | rs7807268 |
ensembl | rs7807268 |
geneview | rs7807268 |
scholar | rs7807268 |
rs7807268 | |
pharmgkb | rs7807268 |
gwascentral | rs7807268 |
openSNP | rs7807268 |
23andMe | rs7807268 |
SNPshot | rs7807268 |
SNPdbe | rs7807268 |
MSV3d | rs7807268 |
GWAS Ctlg | rs7807268 |
GMAF | 0.4931 |
Max Magnitude | 2 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
rs7807268 has been reported in a large study to be associated with Crohn's disease.
The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.38 (CI 1.20-1.60), and for homozygotes, 1.47 (CI 1.24-1.74). [PMID 17554300]
- Note: there is a slight amount of ambiguity over the orientation of this SNP information relative to the dbSNP entry.