rs10789230
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10789230(G;G) |
Make rs10789230(G;T) |
Make rs10789230(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 67264945 |
is a | snp |
is | mentioned by |
dbSNP | rs10789230 |
dbSNP (classic) | rs10789230 |
ClinGen | rs10789230 |
ebi | rs10789230 |
HLI | rs10789230 |
Exac | rs10789230 |
Gnomad | rs10789230 |
Varsome | rs10789230 |
LitVar | rs10789230 |
Map | rs10789230 |
PheGenI | rs10789230 |
Biobank | rs10789230 |
1000 genomes | rs10789230 |
hgdp | rs10789230 |
ensembl | rs10789230 |
geneview | rs10789230 |
scholar | rs10789230 |
rs10789230 | |
pharmgkb | rs10789230 |
gwascentral | rs10789230 |
openSNP | rs10789230 |
23andMe | rs10789230 |
SNPshot | rs10789230 |
SNPdbe | rs10789230 |
MSV3d | rs10789230 |
GWAS Ctlg | rs10789230 |
GMAF | 0.4086 |
Max Magnitude | 0 |
GWAS | |
---|---|
SNP | rs10789230 |
PubMedID | [PMID 17804789] |
Condition | Crohn's disease |
Gene | IL23R |
Risk Allele | |
pValue | 1.00E-008 |
OR | 1.38 |
95% CI | 1.23-1.53 |