PTGFR, prostaglandin F receptor, 5737

N. diseases: 28; N. variants: 8
Disease: Intraocular pressure disorder ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12093097
rs12093097
Entrez Id: 5737
Gene Symbol: PTGFR
PTGFR
CUI: C0595921
Disease:
Intraocular pressure disorder 		0.010 GeneticVariation BEFREE Multiple regression analysis demonstrated that the rs12093097 was the only significant factor that correlated with %ΔIOP (p=0.039). 24457363 2014