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: 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: rs2285666
rs2285666
ACE2
0.925 0.160 X 15592225 splice region variant C/T snv 6.2E-06; 0.28 0.23
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2018 2018
dbSNP: rs2285666
rs2285666
ACE2
0.925 0.160 X 15592225 splice region variant C/T snv 6.2E-06; 0.28 0.23
CUI: C0544618
Disease: Orthostatic hypertension
Orthostatic hypertension 		0.010 1.000 1 2009 2009
dbSNP: rs2285666
rs2285666
ACE2
0.925 0.160 X 15592225 splice region variant C/T snv 6.2E-06; 0.28 0.23
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2012 2012
dbSNP: rs233575
rs233575
ACE2
X 15564843 intron variant G/A snv
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.010 1.000 1 2018 2018
dbSNP: rs35697037
rs35697037
BMX ; ACE2
X 15523993 intron variant G/A snv 0.37
CUI: C0012833
Disease: Dizziness
Dizziness 		0.010 1.000 1 2014 2014
dbSNP: rs35697037
rs35697037
BMX ; ACE2
X 15523993 intron variant G/A snv 0.37
CUI: C0042571
Disease: Vertigo
Vertigo 		0.010 1.000 1 2014 2014
dbSNP: rs4240157
rs4240157
ACE2
0.925 0.080 X 15568841 intron variant C/T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.010 1.000 1 2019 2019
dbSNP: rs4240157
rs4240157
ACE2
0.925 0.080 X 15568841 intron variant C/T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2012 2012
dbSNP: rs4240157
rs4240157
ACE2
0.925 0.080 X 15568841 intron variant C/T snv
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.010 1.000 1 2018 2018
dbSNP: rs4646142
rs4646142
ACE2
X 15584941 intron variant G/A;C 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: 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: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.010 1.000 1 2019 2019
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: 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: 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: rs6632677
rs6632677
ACE2
0.851 0.120 X 15596749 intron variant G/C snv 5.0E-03
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.010 1.000 1 2017 2017
dbSNP: rs6632677
rs6632677
ACE2
0.851 0.120 X 15596749 intron variant G/C snv 5.0E-03
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		0.010 1.000 1 2008 2008