rs10066802
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10066802(A;A) |
Make rs10066802(A;G) |
Make rs10066802(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 77301636 |
Gene | PDE8B |
is a | snp |
is | mentioned by |
dbSNP | rs10066802 |
dbSNP (classic) | rs10066802 |
ClinGen | rs10066802 |
ebi | rs10066802 |
HLI | rs10066802 |
Exac | rs10066802 |
Gnomad | rs10066802 |
Varsome | rs10066802 |
LitVar | rs10066802 |
Map | rs10066802 |
PheGenI | rs10066802 |
Biobank | rs10066802 |
1000 genomes | rs10066802 |
hgdp | rs10066802 |
ensembl | rs10066802 |
geneview | rs10066802 |
scholar | rs10066802 |
rs10066802 | |
pharmgkb | rs10066802 |
gwascentral | rs10066802 |
openSNP | rs10066802 |
23andMe | rs10066802 |
SNPshot | rs10066802 |
SNPdbe | rs10066802 |
MSV3d | rs10066802 |
GWAS Ctlg | rs10066802 |
GMAF | 0.438 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22781450] [Association analysis of PDE8B gene polymorphisms with the susceptibility to Hyperthyroxinemia in Chinese Han population]