Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 10
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 10
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 10
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 9
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 8
rs3755319
UGT1A8 ; UGT1A1 ; UGT1A3 ; UGT1A4 ; UGT1A7 ; UGT1A10 ; UGT1A9 ; UGT1A5 ; UGT1A6
0.925 0.120 2 233758936 intron variant A/C;G;T snv 8
rs4124874
UGT1A5 ; UGT1A4 ; UGT1A7 ; LOC100286922 ; UGT1A8 ; UGT1A10 ; UGT1A3 ; UGT1A6 ; UGT1A9
0.851 0.120 2 233757013 intron variant T/A;G snv 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs643434
ABO
9 133266942 intron variant A/G;T snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 7
rs1875263
UGT1A9 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A6 ; UGT1A8 ; UGT1A4
1.000 2 233716976 intron variant C/G;T snv 7
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs7499892
CETP
16 56972678 intron variant C/G;T snv 7
rs10173355
UGT1A9 ; UGT1A7 ; UGT1A10 ; UGT1A8
1.000 2 233688675 intron variant A/G;T snv 6
rs10750097
APOA5
1.000 0.040 11 116793324 upstream gene variant G/A;C snv 6
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 6
rs4665987 0.925 0.120 2 27532958 upstream gene variant G/A;T snv 6
rs4666002
ZNF512
0.925 0.120 2 27617773 intron variant G/A;C snv 6
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 6