rs12142375
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12142375(A;A) |
Make rs12142375(A;G) |
Make rs12142375(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 66281101 |
Gene | PDE4B |
is a | snp |
is | mentioned by |
dbSNP | rs12142375 |
dbSNP (classic) | rs12142375 |
ClinGen | rs12142375 |
ebi | rs12142375 |
HLI | rs12142375 |
Exac | rs12142375 |
Gnomad | rs12142375 |
Varsome | rs12142375 |
LitVar | rs12142375 |
Map | rs12142375 |
PheGenI | rs12142375 |
Biobank | rs12142375 |
1000 genomes | rs12142375 |
hgdp | rs12142375 |
ensembl | rs12142375 |
geneview | rs12142375 |
scholar | rs12142375 |
rs12142375 | |
pharmgkb | rs12142375 |
gwascentral | rs12142375 |
openSNP | rs12142375 |
23andMe | rs12142375 |
SNPshot | rs12142375 |
SNPdbe | rs12142375 |
MSV3d | rs12142375 |
GWAS Ctlg | rs12142375 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 29061142] Systematic identification of regulatory variants associated with cancer risk.