rs117633859
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs117633859(A;A) |
Make rs117633859(A;G) |
Make rs117633859(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 67162145 |
Gene | IL23R |
is a | snp |
is | mentioned by |
dbSNP | rs117633859 |
dbSNP (classic) | rs117633859 |
ClinGen | rs117633859 |
ebi | rs117633859 |
HLI | rs117633859 |
Exac | rs117633859 |
Gnomad | rs117633859 |
Varsome | rs117633859 |
LitVar | rs117633859 |
Map | rs117633859 |
PheGenI | rs117633859 |
Biobank | rs117633859 |
1000 genomes | rs117633859 |
hgdp | rs117633859 |
ensembl | rs117633859 |
geneview | rs117633859 |
scholar | rs117633859 |
rs117633859 | |
pharmgkb | rs117633859 |
gwascentral | rs117633859 |
openSNP | rs117633859 |
23andMe | rs117633859 |
SNPshot | rs117633859 |
SNPdbe | rs117633859 |
MSV3d | rs117633859 |
GWAS Ctlg | rs117633859 |
Max Magnitude | 0 |
[PMID 25108386] Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3