rs10737680, CFH

N. diseases: 9
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.
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.827 0.080 1 196710325 intron variant A/C snv 0.44 0.800 1.000 4 2010 2013
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.827 0.080 1 196710325 intron variant A/C snv 0.44 0.700 1.000 1 2015 2015
Complement factor H measurement
CUI: C0523353
Disease: Complement factor H measurement
5 0.827 0.080 1 196710325 intron variant A/C snv 0.44 0.700 1.000 1 2017 2017
Exudative age-related macular degeneration
CUI: C0271084
Disease: Exudative age-related macular degeneration
109 0.827 0.080 1 196710325 intron variant A/C snv 0.44 0.700 1.000 1 2015 2015
exudative macular degeneration
CUI: C2237660
Disease: exudative macular degeneration
69 0.827 0.080 1 196710325 intron variant A/C snv 0.44 0.700 1.000 1 2015 2015
response to bronchodilator
CUI: C3548479
Disease: response to bronchodilator
1106 0.827 0.080 1 196710325 intron variant A/C snv 0.44 0.700 1.000 1 2015 2015
Vital capacity
CUI: C0042834
Disease: Vital capacity
746 0.827 0.080 1 196710325 intron variant A/C snv 0.44 0.700 1.000 1 2019 2019
von Willebrand's factor (lab test)
CUI: C2239219
Disease: von Willebrand's factor (lab test)
427 0.827 0.080 1 196710325 intron variant A/C snv 0.44 0.700 1.000 1 2013 2013
Geographic Atrophy
CUI: C1536085
Disease: Geographic Atrophy
81 0.827 0.080 1 196710325 intron variant A/C snv 0.44 0.010 1.000 1 2016 2016