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: rs1260326
rs1260326
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 8 2010 2019
dbSNP: rs7412
rs7412
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 8 2012 2019
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 8 2010 2019
dbSNP: rs12916
rs12916
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 7 2010 2019
dbSNP: rs12740374
rs12740374
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 6 2012 2019
dbSNP: rs2954029
rs2954029
0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 6 2010 2019
dbSNP: rs3764261
rs3764261
0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 6 2010 2019
dbSNP: rs629301
rs629301
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 6 2010 2019
dbSNP: rs646776
rs646776
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 6 2009 2019
dbSNP: rs9987289
rs9987289
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 6 2010 2019
dbSNP: rs1367117
rs1367117
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 5 2010 2019
dbSNP: rs6511720
rs6511720
0.790 0.120 19 11091630 intron variant G/T snv 0.12
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 5 2010 2019
dbSNP: rs6882076
rs6882076
0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 5 2010 2019
dbSNP: rs11207995
rs11207995
1 62583880 intron variant A/C;G snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2013 2019
dbSNP: rs11591147
rs11591147
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2012 2019
dbSNP: rs1564348
rs1564348
6 160157828 intron variant T/C snv 0.14
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2010 2019
dbSNP: rs174546
rs174546
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2010 2019
dbSNP: rs2131925
rs2131925
1 62560271 intron variant G/T snv 0.57
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2010 2019
dbSNP: rs2255141
rs2255141
10 112174128 intron variant A/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2010 2019
dbSNP: rs2297991
rs2297991
10 112153464 3 prime UTR variant T/C snv 0.69
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 4 2015 2019
dbSNP: rs4299376
rs4299376
0.851 0.120 2 43845437 intron variant G/C;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2010 2019
dbSNP: rs507666
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2013 2019
dbSNP: rs562338
rs562338
0.807 0.160 2 21065449 intergenic variant A/G snv 0.69
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2012 2019
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2013 2019
dbSNP: rs7528419
rs7528419
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2012 2019