rs16878037
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16878037(C;C) |
Make rs16878037(C;T) |
Make rs16878037(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 60413925 |
Gene | PDE4D |
is a | snp |
is | mentioned by |
dbSNP | rs16878037 |
dbSNP (classic) | rs16878037 |
ClinGen | rs16878037 |
ebi | rs16878037 |
HLI | rs16878037 |
Exac | rs16878037 |
Gnomad | rs16878037 |
Varsome | rs16878037 |
LitVar | rs16878037 |
Map | rs16878037 |
PheGenI | rs16878037 |
Biobank | rs16878037 |
1000 genomes | rs16878037 |
hgdp | rs16878037 |
ensembl | rs16878037 |
geneview | rs16878037 |
scholar | rs16878037 |
rs16878037 | |
pharmgkb | rs16878037 |
gwascentral | rs16878037 |
openSNP | rs16878037 |
23andMe | rs16878037 |
SNPshot | rs16878037 |
SNPdbe | rs16878037 |
MSV3d | rs16878037 |
GWAS Ctlg | rs16878037 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24926854] Polymorphisms in PDE4D are Associated with a Risk of COPD in Non-Emphysematous Koreans