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: rs17238540
rs17238540
1.000 0.040 5 75359673 non coding transcript exon variant T/G snv 4.0E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 1.000 1 2008 2008
dbSNP: rs17238540
rs17238540
1.000 0.040 5 75359673 non coding transcript exon variant T/G snv 4.0E-02
CUI: C0011847
Disease: Diabetes
Diabetes
0.010 1.000 1 2008 2008
dbSNP: rs3761740
rs3761740
0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 1.000 1 2010 2010
dbSNP: rs3761740
rs3761740
0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 1.000 1 2013 2013
dbSNP: rs3761740
rs3761740
0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2009 2009
dbSNP: rs3761740
rs3761740
0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.010 1.000 1 2013 2013
dbSNP: rs4629571
rs4629571
0.925 0.160 5 75362479 intron variant A/G snv 8.7E-02
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.010 1.000 1 2010 2010
dbSNP: rs4629571
rs4629571
0.925 0.160 5 75362479 intron variant A/G snv 8.7E-02
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
0.010 1.000 1 2010 2010
dbSNP: rs3761739
rs3761739
5 75335676 intron variant C/T snv 0.15
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs3761739
rs3761739
5 75335676 intron variant C/T snv 0.15
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs3761739
rs3761739
5 75335676 intron variant C/T snv 0.15
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs10474434
rs10474434
5 75348856 intron variant G/T snv 0.20
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs10474434
rs10474434
5 75348856 intron variant G/T snv 0.20
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs10474434
rs10474434
5 75348856 intron variant G/T snv 0.20
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs17238484
rs17238484
1.000 0.080 5 75352671 intron variant G/T snv 0.22
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2015 2015
dbSNP: rs17238484
rs17238484
1.000 0.080 5 75352671 intron variant G/T snv 0.22
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs17238484
rs17238484
1.000 0.080 5 75352671 intron variant G/T snv 0.22
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs17238484
rs17238484
1.000 0.080 5 75352671 intron variant G/T snv 0.22
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs10045497
rs10045497
5 75340659 intron variant C/A snv 0.35
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2013 2013
dbSNP: rs10045497
rs10045497
5 75340659 intron variant C/A snv 0.35
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2013 2013
dbSNP: rs3843482
rs3843482
5 75343434 intron variant T/G snv 0.35
Low density lipoprotein cholesterol measurement
0.700 1.000 3 2015 2019
dbSNP: rs3843482
rs3843482
5 75343434 intron variant T/G snv 0.35
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs3846663
rs3846663
0.882 0.120 5 75359901 intron variant C/T snv 0.35
Low density lipoprotein cholesterol measurement
0.800 1.000 3 2009 2019
dbSNP: rs3846663
rs3846663
0.882 0.120 5 75359901 intron variant C/T snv 0.35
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2019 2019
dbSNP: rs3846663
rs3846663
0.882 0.120 5 75359901 intron variant C/T snv 0.35
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011