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: rs12916
rs12916
0.878 0.143 5 75360714 3 prime UTR variant T/C snp 0.38
Low density lipoprotein cholesterol measurement
0.800 6 2010 2017
dbSNP: rs12916
rs12916
0.878 0.143 5 75360714 3 prime UTR variant T/C snp 0.38
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 5 2010 2017
dbSNP: rs12654264
rs12654264
0.878 0.107 5 75352778 intron variant A/T snp 0.39
Low density lipoprotein cholesterol measurement
0.800 3 2008 2012
dbSNP: rs3846662
rs3846662
0.821 0.250 5 75355259 non coding transcript exon variant A/G snp 0.50 0.58
Low density lipoprotein cholesterol measurement
0.800 3 2009 2013
dbSNP: rs10038095
rs10038095
5 75341886 intron variant A/T snp 0.39
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 2 2012 2015
dbSNP: rs3846662
rs3846662
0.821 0.250 5 75355259 non coding transcript exon variant A/G snp 0.50 0.58
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 2 2009 2012
dbSNP: rs10045497
rs10045497
5 75340659 intron variant C/A snp 0.36
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1 2013 2013
dbSNP: rs3846663
rs3846663
1.000 0.036 5 75359901 intron variant C/T snp 0.37
Low density lipoprotein cholesterol measurement
0.800 1 2009 2009
dbSNP: rs10038095
rs10038095
5 75341886 intron variant A/T snp 0.39
Low density lipoprotein cholesterol measurement
0.700 1 2012 2012
dbSNP: rs10045497
rs10045497
5 75340659 intron variant C/A snp 0.36
Low density lipoprotein cholesterol measurement
0.700 1 2013 2013
dbSNP: rs10474434
rs10474434
5 75348856 intron variant G/T snp 0.20
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1 2012 2012
dbSNP: rs10474434
rs10474434
5 75348856 intron variant G/T snp 0.20
Low density lipoprotein cholesterol measurement
0.700 1 2012 2012
dbSNP: rs12654264
rs12654264
0.878 0.107 5 75352778 intron variant A/T snp 0.39
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1 2011 2011
dbSNP: rs12654264
rs12654264
0.878 0.107 5 75352778 intron variant A/T snp 0.39
LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 3
0.700 1 2008 2008
dbSNP: rs12654264
rs12654264
0.878 0.107 5 75352778 intron variant A/T snp 0.39
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1 2012 2012
dbSNP: rs12654264
rs12654264
0.878 0.107 5 75352778 intron variant A/T snp 0.39
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1 2011 2011
dbSNP: rs17238484
rs17238484
1.000 0.071 5 75352671 intron variant G/T snp 0.23
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1 2012 2012
dbSNP: rs17238484
rs17238484
1.000 0.071 5 75352671 intron variant G/T snp 0.23
Low density lipoprotein cholesterol measurement
0.700 1 2012 2012
dbSNP: rs3761739
rs3761739
5 75335676 intron variant C/T snp 0.16
Low density lipoprotein cholesterol measurement
0.700 1 2012 2012
dbSNP: rs3761739
rs3761739
5 75335676 intron variant C/T snp 0.16
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1 2012 2012
dbSNP: rs3761740
rs3761740
1.000 0.071 5 75336308 intron variant C/A snp 8.1E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1 2009 2009
dbSNP: rs3843482
rs3843482
5 75343434 intron variant T/G snp 0.37
Low density lipoprotein cholesterol measurement
0.700 1 2015 2015
dbSNP: rs3846662
rs3846662
0.821 0.250 5 75355259 non coding transcript exon variant A/G snp 0.50 0.58
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.700 1 2013 2013
dbSNP: rs3846662
rs3846662
0.821 0.250 5 75355259 non coding transcript exon variant A/G snp 0.50 0.58
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1 2011 2011
dbSNP: rs3846663
rs3846663
1.000 0.036 5 75359901 intron variant C/T snp 0.37
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1 2011 2011