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: 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: 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: 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: rs3846661
rs3846661
5 75343353 intron variant A/G snv 0.56
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs3846662
rs3846662
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs3846662
rs3846662
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2012 2012
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
dbSNP: rs3846663
rs3846663
0.882 0.120 5 75359901 intron variant C/T snv 0.35
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2009 2009
dbSNP: rs3846663
rs3846663
0.882 0.120 5 75359901 intron variant C/T snv 0.35
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2009 2009
dbSNP: rs6453131
rs6453131
5 75348881 intron variant T/G snv 0.39
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs6453131
rs6453131
5 75348881 intron variant T/G snv 0.39
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs6453131
rs6453131
5 75348881 intron variant T/G snv 0.39
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs12654264
rs12654264
0.925 0.120 5 75352778 intron variant A/T snv 0.38
LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 3
0.700 0
dbSNP: rs3846662
rs3846662
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.050 1.000 5 2015 2019
dbSNP: rs12916
rs12916
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.020 1.000 2 2016 2018
dbSNP: rs12916
rs12916
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.020 1.000 2 2016 2018
dbSNP: rs3846662
rs3846662
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
0.020 0.500 2 2019 2019
dbSNP: rs12654264
rs12654264
0.925 0.120 5 75352778 intron variant A/T snv 0.38
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs12916
rs12916
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal
0.010 1.000 1 2018 2018
dbSNP: rs12916
rs12916
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2018 2018
dbSNP: rs12916
rs12916
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2015 2015
dbSNP: rs12916
rs12916
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2018 2018