rs8177179, INHCAP;TF

N. diseases: 4
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.
Serum transferrin measurement
CUI: C0428545
Disease: Serum transferrin measurement
10 0.925 0.080 3 133744613 intron variant G/A snv 0.58 0.700 1.000 1 2014 2014
Transferrin measurement
CUI: C0202105
Disease: Transferrin measurement
10 0.925 0.080 3 133744613 intron variant G/A snv 0.58 0.700 1.000 1 2014 2014
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.925 0.080 3 133744613 intron variant G/A snv 0.58 0.010 1.000 1 2013 2013
Fuchs Endothelial Dystrophy
CUI: C0016781
Disease: Fuchs Endothelial Dystrophy
32 0.925 0.080 3 133744613 intron variant G/A snv 0.58 0.010 1.000 1 2013 2013