rs9988642
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9988642(C;C) |
Make rs9988642(C;T) |
Make rs9988642(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 67260421 |
Gene | IL23R |
is a | snp |
is | mentioned by |
dbSNP | rs9988642 |
dbSNP (classic) | rs9988642 |
ClinGen | rs9988642 |
ebi | rs9988642 |
HLI | rs9988642 |
Exac | rs9988642 |
Gnomad | rs9988642 |
Varsome | rs9988642 |
LitVar | rs9988642 |
Map | rs9988642 |
PheGenI | rs9988642 |
Biobank | rs9988642 |
1000 genomes | rs9988642 |
hgdp | rs9988642 |
ensembl | rs9988642 |
geneview | rs9988642 |
scholar | rs9988642 |
rs9988642 | |
pharmgkb | rs9988642 |
gwascentral | rs9988642 |
openSNP | rs9988642 |
23andMe | rs9988642 |
SNPshot | rs9988642 |
SNPdbe | rs9988642 |
MSV3d | rs9988642 |
GWAS Ctlg | rs9988642 |
GMAF | 0.1084 |
Max Magnitude | 0 |
GWAS | |
---|---|
SNP | rs9988642 |
PubMedID | [PMID 17804789] |
Condition | Crohn's disease |
Gene | IL23R |
Risk Allele | |
pValue | 1.00E-008 |
OR | 1.38 |
95% CI | 1.23-1.53 |