Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 16
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 15
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs6854845 0.827 0.080 4 74821455 intergenic variant G/T snv 0.13 6
rs2853668 0.882 0.080 5 1299910 upstream gene variant G/T snv 0.33 5
rs3093075 0.882 0.120 1 159710123 upstream gene variant G/T snv 0.13 5
rs2770150 0.925 0.080 9 117700861 upstream gene variant A/G snv 0.22 4
rs997476 0.882 0.080 4 102620848 downstream gene variant G/T snv 4.3E-02 3
rs1365611 0.925 0.080 4 174462542 intergenic variant C/T snv 0.28 2
rs2332897 0.925 0.080 4 174465154 intergenic variant C/A;G snv 0.29 2
rs6844282 0.925 0.080 4 174460480 regulatory region variant C/A;G snv 2
rs12527379 1.000 0.080 6 131958700 intron variant G/A snv 0.31 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs41395947
ABCC1
0.925 0.080 16 16007895 missense variant G/C snv 2.0E-05 7.0E-06 2
rs41494447
ABCC1
0.925 0.080 16 16007985 missense variant C/T snv 4.4E-04 2.2E-04 2
rs8086
ACSL1
0.925 0.080 4 184756267 3 prime UTR variant C/T snv 0.24 2
rs3811802
ADH1B
0.925 0.080 4 99323064 intron variant A/C;G;T snv 2
rs4147536
ADH1B
0.925 0.080 4 99317955 non coding transcript exon variant A/C snv 0.71 2
rs4147542
ADH1C ; ADH1B
0.882 0.160 4 99347396 intron variant T/C snv 0.33 3
rs283415
ADH1C ; ADH1B
0.925 0.080 4 99349450 intron variant C/T snv 0.64 2
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37