rs10033900, CFI

N. diseases: 7
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.
Polypoidal choroidal vasculopathy
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
67 0.807 0.040 4 109737911 intron variant T/C snv 0.54 0.010 1.000 1 2014 2014
exudative macular degeneration
CUI: C2237660
Disease: exudative macular degeneration
69 0.807 0.040 4 109737911 intron variant T/C snv 0.54 0.700 1.000 2 2012 2016
Geographic Atrophy
CUI: C1536085
Disease: Geographic Atrophy
81 0.807 0.040 4 109737911 intron variant T/C snv 0.54 0.700 1.000 1 2016 2016
Exudative age-related macular degeneration
109 0.807 0.040 4 109737911 intron variant T/C snv 0.54 0.710 1.000 3 2012 2016
Myopia
CUI: C0027092
Disease: Myopia
167 0.807 0.040 4 109737911 intron variant T/C snv 0.54 0.010 1.000 1 2012 2012
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.807 0.040 4 109737911 intron variant T/C snv 0.54 0.840 0.875 8 2010 2019
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.807 0.040 4 109737911 intron variant T/C snv 0.54 0.700 1.000 1 2018 2018