rs7702192
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7702192(A;A) |
Make rs7702192(A;C) |
Make rs7702192(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 77258982 |
Gene | PDE8B |
is a | snp |
is | mentioned by |
dbSNP | rs7702192 |
dbSNP (classic) | rs7702192 |
ClinGen | rs7702192 |
ebi | rs7702192 |
HLI | rs7702192 |
Exac | rs7702192 |
Gnomad | rs7702192 |
Varsome | rs7702192 |
LitVar | rs7702192 |
Map | rs7702192 |
PheGenI | rs7702192 |
Biobank | rs7702192 |
1000 genomes | rs7702192 |
hgdp | rs7702192 |
ensembl | rs7702192 |
geneview | rs7702192 |
scholar | rs7702192 |
rs7702192 | |
pharmgkb | rs7702192 |
gwascentral | rs7702192 |
openSNP | rs7702192 |
23andMe | rs7702192 |
SNPshot | rs7702192 |
SNPdbe | rs7702192 |
MSV3d | rs7702192 |
GWAS Ctlg | rs7702192 |
GMAF | 0.4624 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 22781450] [Association analysis of PDE8B gene polymorphisms with the susceptibility to Hyperthyroxinemia in Chinese Han population]