rs3766355, PTGFR

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Glaucoma
CUI: C0017601
Disease: Glaucoma
198 0.882 0.040 1 78491756 intron variant C/A;T snv 0.010 1.000 1 2016 2016