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: rs4393158
rs4393158
1.000 0.040 1 209678552 intron variant A/G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2014 2014
dbSNP: rs4393158
rs4393158
1.000 0.040 1 209678552 intron variant A/G;T snv
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.010 1.000 1 2014 2014
dbSNP: rs846908
rs846908
1.000 0.120 1 209685108 intron variant A/G snv 0.97
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.010 1.000 1 2015 2015
dbSNP: rs2235543
rs2235543
0.925 0.080 1 209687323 intron variant T/A;C snv
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.010 1.000 1 2014 2014
dbSNP: rs2235543
rs2235543
0.925 0.080 1 209687323 intron variant T/A;C snv
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.010 1.000 1 2016 2016
dbSNP: rs2235543
rs2235543
0.925 0.080 1 209687323 intron variant T/A;C snv
CUI: C0852036
Disease: Pregnancy associated hypertension
Pregnancy associated hypertension
0.010 1.000 1 2013 2013
dbSNP: rs2235543
rs2235543
0.925 0.080 1 209687323 intron variant T/A;C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2014 2014
dbSNP: rs12565406
rs12565406
1.000 0.040 1 209687741 intron variant G/A;T snv
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.010 1.000 1 2016 2016
dbSNP: rs10082248
rs10082248
1.000 0.080 1 209693771 intron variant A/G;T snv
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2014 2014
dbSNP: rs4844880
rs4844880
0.882 0.240 1 209697571 intron variant A/T snv 0.70
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
0.010 1.000 1 2015 2015
dbSNP: rs4844880
rs4844880
0.882 0.240 1 209697571 intron variant A/T snv 0.70
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.010 1.000 1 2016 2016
dbSNP: rs4844880
rs4844880
0.882 0.240 1 209697571 intron variant A/T snv 0.70
CUI: C0029458
Disease: Osteoporosis, Postmenopausal
Osteoporosis, Postmenopausal
0.010 1.000 1 2012 2012
dbSNP: rs4844880
rs4844880
0.882 0.240 1 209697571 intron variant A/T snv 0.70
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.010 1.000 1 2014 2014
dbSNP: rs846910
rs846910
0.882 0.160 1 209701909 intron variant A/G snv 0.95
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.020 1.000 2 2011 2017
dbSNP: rs846910
rs846910
0.882 0.160 1 209701909 intron variant A/G snv 0.95
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2017 2017
dbSNP: rs846910
rs846910
0.882 0.160 1 209701909 intron variant A/G snv 0.95
CUI: C1392786
Disease: Cognitive changes
Cognitive changes
0.010 1.000 1 2006 2006
dbSNP: rs846910
rs846910
0.882 0.160 1 209701909 intron variant A/G snv 0.95
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2004 2004
dbSNP: rs846910
rs846910
0.882 0.160 1 209701909 intron variant A/G snv 0.95
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.010 1.000 1 2011 2011
dbSNP: rs846910
rs846910
0.882 0.160 1 209701909 intron variant A/G snv 0.95
CUI: C0852036
Disease: Pregnancy associated hypertension
Pregnancy associated hypertension
0.010 1.000 1 2013 2013
dbSNP: rs3753519
rs3753519
0.925 0.200 1 209702170 intron variant T/A;C snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.010 1.000 1 2014 2014
dbSNP: rs3753519
rs3753519
0.925 0.200 1 209702170 intron variant T/A;C snv
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2012 2012
dbSNP: rs846911
rs846911
1.000 0.080 1 209702906 intron variant C/A snv 9.3E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 1.000 1 2006 2006
dbSNP: rs45487298
rs45487298
0.882 0.120 1 209706871 intron variant -/A delins
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2019 2019
dbSNP: rs45487298
rs45487298
0.882 0.120 1 209706871 intron variant -/A delins
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.010 1.000 1 2019 2019
dbSNP: rs45487298
rs45487298
0.882 0.120 1 209706871 intron variant -/A delins
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.010 1.000 1 2015 2015