rs12603825
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12603825(A;A) |
Make rs12603825(A;G) |
Make rs12603825(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 1770111 |
Gene | SERPINF1 |
is a | snp |
is | mentioned by |
dbSNP | rs12603825 |
dbSNP (classic) | rs12603825 |
ClinGen | rs12603825 |
ebi | rs12603825 |
HLI | rs12603825 |
Exac | rs12603825 |
Gnomad | rs12603825 |
Varsome | rs12603825 |
LitVar | rs12603825 |
Map | rs12603825 |
PheGenI | rs12603825 |
Biobank | rs12603825 |
1000 genomes | rs12603825 |
hgdp | rs12603825 |
ensembl | rs12603825 |
geneview | rs12603825 |
scholar | rs12603825 |
rs12603825 | |
pharmgkb | rs12603825 |
gwascentral | rs12603825 |
openSNP | rs12603825 |
23andMe | rs12603825 |
SNPshot | rs12603825 |
SNPdbe | rs12603825 |
MSV3d | rs12603825 |
GWAS Ctlg | rs12603825 |
GMAF | 0.3095 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21439646] Genetic variants in pigment epithelium-derived factor influence response of polypoidal choroidal vasculopathy to photodynamic therapy
[PMID 22457810] Common Genetic Variation in the SERPINF1 Locus Determines Overall Adiposity, Obesity-Related Insulin Resistance, and Circulating Leptin Levels
[PMID 23722394] Evaluation of pigment epithelium-derived factor and complement factor I polymorphisms as a cause of choroidal neovascularization in highly myopic eyes
[PMID 28420811] The T Allele of rs8075977 in the 5'-Flanking Region of the PEDF Gene Is Associated with Reduced Risk of Coronary Artery Disease in Elderly Chinese Men.