Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 7
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs35444 12 115114632 intergenic variant A/G snv 0.38 6
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 6
rs1173766 5 32804422 intergenic variant T/C snv 0.57 5
rs13082711 3 27496418 intergenic variant T/C snv 0.16 5
rs13209747 6 126794309 intron variant C/G;T snv 0.36 5
rs16849225 2 164050310 intron variant C/T snv 0.19 5
rs2954033 8 125481504 intron variant A/G snv 0.76 5
rs1446468 2 164106976 intron variant T/C snv 0.40 4
rs17477177 1.000 0.080 7 106771412 upstream gene variant T/C snv 0.17 4
rs12627514 1.000 0.040 21 43339560 intergenic variant C/A;G;T snv 3
rs13002573 2 164058698 intron variant A/G snv 0.20 3
rs16833934 3 164019462 intergenic variant A/G snv 0.34 3
rs17428471 7 27298248 intergenic variant G/T snv 9.4E-02 3
rs2969070 7 2472910 downstream gene variant G/A;C snv 3
rs4842666 12 89547772 non coding transcript exon variant T/C snv 0.16 3
rs871606 4 53933078 intron variant T/C;G snv 3
rs13040716 1.000 0.040 20 32182402 downstream gene variant A/G snv 1.0E-01 2
rs16877320 6 15922795 TF binding site variant T/A;C snv 2