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: rs287354
rs287354
13 68665820 intergenic variant A/G snv 0.61
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2007 2007
dbSNP: rs287474
rs287474
13 68701828 intergenic variant T/A snv 0.58
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2007 2007
dbSNP: rs4982795
rs4982795
14 23755826 downstream gene variant T/C snv 0.38
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2007 2007
dbSNP: rs524802
rs524802
19 36956045 intron variant G/A snv 0.36
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2007 2007
dbSNP: rs7231460
rs7231460
18 31252224 intergenic variant T/C snv 0.42
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2007 2007
dbSNP: rs966376
rs966376
18 31252875 intergenic variant T/C snv 0.41
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2007 2007
dbSNP: rs12272004
rs12272004
1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2009 2009
dbSNP: rs6756629
rs6756629
0.925 0.080 2 43837951 missense variant G/A;T snv 6.7E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2009 2009
dbSNP: rs6987702
rs6987702
8 125492484 intron variant T/C snv 0.43
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2009 2009
dbSNP: rs2737229
rs2737229
8 115636338 intron variant A/C snv 0.48
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2010 2010
dbSNP: rs15892
rs15892
7 55955288 3 prime UTR variant T/C snv 0.82
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2011 2011
dbSNP: rs16981145
rs16981145
20 19809906 intron variant G/C snv 0.14
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2011 2011
dbSNP: rs17026635
rs17026635
1 216379025 intron variant C/T snv 0.12
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2011 2011
dbSNP: rs4679788
rs4679788
3 157236602 intron variant T/C snv 0.20
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2011 2011
dbSNP: rs4742455
rs4742455
9 8118541 intergenic variant C/T snv 0.45
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2011 2011
dbSNP: rs6448771
rs6448771
4 31395996 intergenic variant G/A;C snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2011 2011
dbSNP: rs6987225
rs6987225
8 97963444 intron variant A/C snv 8.7E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2011 2011
dbSNP: rs7790255
rs7790255
7 55901572 intron variant G/A;C snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2011 2011
dbSNP: rs283813
rs283813
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2012 2012
dbSNP: rs10047462
rs10047462
11 116851325 intron variant G/C;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs10115928
rs10115928
9 104888562 intron variant C/T snv 0.47
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs10156121
rs10156121
7 142672656 downstream gene variant T/C snv 3.9E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs10199768
rs10199768
2 21021128 intron variant G/T snv 0.35
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs10220503
rs10220503
14 74480389 3 prime UTR variant C/A snv 1.1E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs102275
rs102275
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012