rs17514846, FURIN

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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.120 15 90873320 intron variant C/A;G snv 0.810 1.000 4 2013 2018
Mean blood pressure
CUI: C0428886
Disease: Mean blood pressure
344 0.882 0.120 15 90873320 intron variant C/A;G snv 0.700 1.000 2 2016 2018
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.882 0.120 15 90873320 intron variant C/A;G snv 0.700 1.000 2 2018 2019
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.882 0.120 15 90873320 intron variant C/A;G snv 0.700 1.000 2 2018 2018
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
35 0.882 0.120 15 90873320 intron variant C/A;G snv 0.700 1.000 1 2013 2013
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.120 15 90873320 intron variant C/A;G snv 0.700 1.000 1 2018 2018
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.882 0.120 15 90873320 intron variant C/A;G snv 0.010 1.000 1 2015 2015