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rs12603825

From SNPedia

Orientationplus
Stabilizedplus
Make rs12603825(A;A)
Make rs12603825(A;G)
Make rs12603825(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position1770111
GeneSERPINF1
is asnp
is mentioned by
dbSNPrs12603825
dbSNP (classic)rs12603825
ClinGenrs12603825
ebirs12603825
HLIrs12603825
Exacrs12603825
Gnomadrs12603825
Varsomers12603825
LitVarrs12603825
Maprs12603825
PheGenIrs12603825
Biobankrs12603825
1000 genomesrs12603825
hgdprs12603825
ensemblrs12603825
geneviewrs12603825
scholarrs12603825
googlers12603825
pharmgkbrs12603825
gwascentralrs12603825
openSNPrs12603825
23andMers12603825
SNPshotrs12603825
SNPdbers12603825
MSV3drs12603825
GWAS Ctlgrs12603825
GMAF0.3095
Max Magnitude0
? (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 22457810OA-icon.png] 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.