Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 11
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
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 10
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 8
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 7
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 7
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 6
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 6