rs6669582
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6669582(A;A) |
Make rs6669582(A;G) |
Make rs6669582(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 67264372 |
is a | snp |
is | mentioned by |
dbSNP | rs6669582 |
dbSNP (classic) | rs6669582 |
ClinGen | rs6669582 |
ebi | rs6669582 |
HLI | rs6669582 |
Exac | rs6669582 |
Gnomad | rs6669582 |
Varsome | rs6669582 |
LitVar | rs6669582 |
Map | rs6669582 |
PheGenI | rs6669582 |
Biobank | rs6669582 |
1000 genomes | rs6669582 |
hgdp | rs6669582 |
ensembl | rs6669582 |
geneview | rs6669582 |
scholar | rs6669582 |
rs6669582 | |
pharmgkb | rs6669582 |
gwascentral | rs6669582 |
openSNP | rs6669582 |
23andMe | rs6669582 |
SNPshot | rs6669582 |
SNPdbe | rs6669582 |
MSV3d | rs6669582 |
GWAS Ctlg | rs6669582 |
GMAF | 0.2805 |
Max Magnitude | 0 |
GWAS | |
---|---|
SNP | rs6669582 |
PubMedID | [PMID 17804789] |
Condition | Crohn's disease |
Gene | IL23R |
Risk Allele | |
pValue | 1.00E-008 |
OR | 1.38 |
95% CI | 1.23-1.53 |