Source: BEFREE

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: rs2106809
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.040 1.000 4 2014 2019
dbSNP: rs2106809
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.020 1.000 2 2007 2016
dbSNP: rs4646188
rs4646188
ACE2
0.925 0.120 X 15583220 intron variant A/G snv 9.1E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.020 1.000 2 2012 2018
dbSNP: rs4646188
rs4646188
ACE2
0.925 0.120 X 15583220 intron variant A/G snv 9.1E-02
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.020 1.000 2 2018 2019
dbSNP: rs4646188
rs4646188
ACE2
0.925 0.120 X 15583220 intron variant A/G snv 9.1E-02
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.020 0.500 2 2018 2018
dbSNP: rs1514280
rs1514280
ACE2
1.000 X 15568325 intron variant A/G snv
CUI: C0749263
Disease: temporal pain
temporal pain 		0.010 1.000 1 2013 2013
dbSNP: rs1514280
rs1514280
ACE2
1.000 X 15568325 intron variant A/G snv
CUI: C0233397
Disease: Psychological symptom
Psychological symptom 		0.010 1.000 1 2013 2013
dbSNP: rs1514280
rs1514280
ACE2
1.000 X 15568325 intron variant A/G snv
CUI: C4531100
Disease: Negative affectivity
Negative affectivity 		0.010 1.000 1 2013 2013
dbSNP: rs2106809
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy 		0.010 1.000 1 2019 2019
dbSNP: rs2106809
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		0.010 1.000 1 2008 2008
dbSNP: rs2106809
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19
CUI: C0741923
Disease: cardiac event
cardiac event 		0.010 1.000 1 2013 2013
dbSNP: rs2106809
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 1.000 1 2013 2013
dbSNP: rs2106809
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19
CUI: C0340489
Disease: Lone atrial fibrillation
Lone atrial fibrillation 		0.010 1.000 1 2013 2013
dbSNP: rs2106809
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.010 1.000 1 2018 2018
dbSNP: rs4646188
rs4646188
ACE2
0.925 0.120 X 15583220 intron variant A/G snv 9.1E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2012 2012
dbSNP: rs4646156
rs4646156
ACE2
X 15578920 intron variant A/T snv
CUI: C0002962
Disease: Angina Pectoris
Angina Pectoris 		0.010 1.000 1 2013 2013
dbSNP: rs4646156
rs4646156
ACE2
X 15578920 intron variant A/T snv
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.010 1.000 1 2018 2018
dbSNP: rs879922
rs879922
ACE2
0.882 0.160 X 15572684 intron variant C/G snv
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.030 1.000 3 2018 2019
dbSNP: rs879922
rs879922
ACE2
0.882 0.160 X 15572684 intron variant C/G snv
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.020 1.000 2 2018 2018
dbSNP: rs879922
rs879922
ACE2
0.882 0.160 X 15572684 intron variant C/G snv
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis 		0.010 1.000 1 2018 2018
dbSNP: rs879922
rs879922
ACE2
0.882 0.160 X 15572684 intron variant C/G snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2018 2018
dbSNP: rs4830542
rs4830542
ACE2
0.925 0.080 X 15558483 downstream gene variant C/G;T snv
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.020 1.000 2 2018 2019
dbSNP: rs4830542
rs4830542
ACE2
0.925 0.080 X 15558483 downstream gene variant C/G;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.010 1.000 1 2019 2019
dbSNP: rs4830542
rs4830542
ACE2
0.925 0.080 X 15558483 downstream gene variant C/G;T snv
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.010 1.000 1 2018 2018
dbSNP: rs4646155
rs4646155
ACE2
0.925 0.080 X 15579386 intron variant C/T snv 3.9E-02
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.030 1.000 3 2018 2019