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: rs879922
rs879922
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: rs4240157
rs4240157
0.925 0.080 X 15568841 intron variant C/T snv
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.020 1.000 2 2018 2019
dbSNP: rs4830542
rs4830542
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: rs879922
rs879922
0.882 0.160 X 15572684 intron variant C/G snv
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.020 1.000 2 2018 2018
dbSNP: rs1514280
rs1514280
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
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
1.000 X 15568325 intron variant A/G snv
CUI: C4531100
Disease: Negative affectivity
Negative affectivity
0.010 1.000 1 2013 2013
dbSNP: rs1978124
rs1978124
X 15599940 intron variant T/A;C snv
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.010 1.000 1 2018 2018
dbSNP: rs1978124
rs1978124
X 15599940 intron variant T/A;C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2012 2012
dbSNP: rs2048683
rs2048683
1.000 0.040 X 15590376 intron variant T/G snv
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.010 < 0.001 1 2018 2018
dbSNP: rs233575
rs233575
X 15564843 intron variant G/A snv
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.010 1.000 1 2018 2018
dbSNP: rs4240157
rs4240157
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
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
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
X 15584941 intron variant G/A;C snv
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.010 1.000 1 2018 2018
dbSNP: rs4646156
rs4646156
X 15578920 intron variant A/T snv
CUI: C0002962
Disease: Angina Pectoris
Angina Pectoris
0.010 1.000 1 2013 2013
dbSNP: rs4646156
rs4646156
X 15578920 intron variant A/T snv
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.010 1.000 1 2018 2018
dbSNP: rs4830542
rs4830542
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
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: rs879922
rs879922
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
0.882 0.160 X 15572684 intron variant C/G snv
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2018 2018
dbSNP: rs762890235
rs762890235
0.827 0.240 X 15578220 missense variant G/T snv 3.8E-05 9.5E-06
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 1.000 1 2006 2006
dbSNP: rs762890235
rs762890235
0.827 0.240 X 15578220 missense variant G/T snv 3.8E-05 9.5E-06
Diabetes Mellitus, Insulin-Dependent
0.010 1.000 1 2008 2008
dbSNP: rs762890235
rs762890235
0.827 0.240 X 15578220 missense variant G/T snv 3.8E-05 9.5E-06
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2013 2013
dbSNP: rs762890235
rs762890235
0.827 0.240 X 15578220 missense variant G/T snv 3.8E-05 9.5E-06
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2013 2013