rs206468
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs206468(A;A) |
Make rs206468(A;G) |
Make rs206468(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 10296941 |
is a | snp |
is | mentioned by |
dbSNP | rs206468 |
dbSNP (classic) | rs206468 |
ClinGen | rs206468 |
ebi | rs206468 |
HLI | rs206468 |
Exac | rs206468 |
Gnomad | rs206468 |
Varsome | rs206468 |
LitVar | rs206468 |
Map | rs206468 |
PheGenI | rs206468 |
Biobank | rs206468 |
1000 genomes | rs206468 |
hgdp | rs206468 |
ensembl | rs206468 |
geneview | rs206468 |
scholar | rs206468 |
rs206468 | |
pharmgkb | rs206468 |
gwascentral | rs206468 |
openSNP | rs206468 |
23andMe | rs206468 |
SNPshot | rs206468 |
SNPdbe | rs206468 |
MSV3d | rs206468 |
GWAS Ctlg | rs206468 |
GMAF | 0.3338 |
Max Magnitude | 0 |
GWAS | |
---|---|
SNP | rs11209003,rs11209002,rs206468 |
PubMedID | [PMID 17804789] |
Condition | Crohn's disease |
Gene | IL23R |
Risk Allele | |
pValue | 2.00E-007 |
OR | 2.56 |
95% CI | 1.75-3.70 |