Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17514846
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.810 1.000 4 2013 2018
dbSNP: rs4702
rs4702
FES ; FURIN
1.000 0.040 15 90883330 3 prime UTR variant G/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.720 1.000 7 2014 2019
dbSNP: rs17514846
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 2 2016 2018
dbSNP: rs17514846
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2018 2019
dbSNP: rs17514846
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 2 2018 2018
dbSNP: rs1573643
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs1573643
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1573643
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2018 2018
dbSNP: rs1573643
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs1573643
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs17514846
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.700 1.000 1 2018 2018
dbSNP: rs17514846
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 		0.700 1.000 1 2013 2013
dbSNP: rs2071410
rs2071410
FURIN
0.882 0.160 15 90877710 intron variant C/A;G;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2018 2018
dbSNP: rs2071410
rs2071410
FURIN
0.882 0.160 15 90877710 intron variant C/A;G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs4702
rs4702
FES ; FURIN
1.000 0.040 15 90883330 3 prime UTR variant G/A;C snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs4702
rs4702
FES ; FURIN
1.000 0.040 15 90883330 3 prime UTR variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs8032315
rs8032315
FURIN
1.000 0.040 15 90875067 intron variant T/A snv 0.29
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs8032315
rs8032315
FURIN
1.000 0.040 15 90875067 intron variant T/A snv 0.29
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs8039305
rs8039305
FURIN
15 90879313 intron variant T/C snv 0.55
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.700 1.000 1 2018 2018
dbSNP: rs1040264140
rs1040264140
FURIN
1.000 0.080 15 90881744 missense variant A/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2010 2010
dbSNP: rs1040264140
rs1040264140
FURIN
1.000 0.080 15 90881744 missense variant A/G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2010 2010
dbSNP: rs17514846
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.010 1.000 1 2015 2015
dbSNP: rs2071410
rs2071410
FURIN
0.882 0.160 15 90877710 intron variant C/A;G;T snv
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia 		0.010 1.000 1 2016 2016
dbSNP: rs2071410
rs2071410
FURIN
0.882 0.160 15 90877710 intron variant C/A;G;T snv
CUI: C0007787
Disease: Transient Ischemic Attack
Transient Ischemic Attack 		0.010 1.000 1 2016 2016
dbSNP: rs2071410
rs2071410
FURIN
0.882 0.160 15 90877710 intron variant C/A;G;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.010 1.000 1 2016 2016