rs7746082
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7746082(C;C) |
Make rs7746082(C;G) |
Make rs7746082(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 105987394 |
is a | snp |
is | mentioned by |
dbSNP | rs7746082 |
dbSNP (classic) | rs7746082 |
ClinGen | rs7746082 |
ebi | rs7746082 |
HLI | rs7746082 |
Exac | rs7746082 |
Gnomad | rs7746082 |
Varsome | rs7746082 |
LitVar | rs7746082 |
Map | rs7746082 |
PheGenI | rs7746082 |
Biobank | rs7746082 |
1000 genomes | rs7746082 |
hgdp | rs7746082 |
ensembl | rs7746082 |
geneview | rs7746082 |
scholar | rs7746082 |
rs7746082 | |
pharmgkb | rs7746082 |
gwascentral | rs7746082 |
openSNP | rs7746082 |
23andMe | rs7746082 |
SNPshot | rs7746082 |
SNPdbe | rs7746082 |
MSV3d | rs7746082 |
GWAS Ctlg | rs7746082 |
GMAF | 0.1345 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs7746082 |
PubMedID | [PMID 18587394] |
Condition | Crohn's disease |
Gene | Unknown |
Risk Allele | C |
pValue | 2.00E-010 |
OR | 1.17 |
95% CI |
DeCode reports that rs7746082 is associated with susceptibility to Crohn's disease. [PMID 18587394]
[PMID 21752155] Genetic susceptibility to inflammation and colonic transit in lower functional gastrointestinal disorders: preliminary analysis
[PMID 21304977] An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.