Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 7
rs17411031 0.925 0.120 8 19994799 regulatory region variant C/G snv 0.25 7
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 7
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 6
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs2823139 1.000 0.080 21 15204463 intron variant G/A snv 0.34 5
rs17477177 1.000 0.080 7 106771412 upstream gene variant T/C snv 0.17 4
rs2770150 0.925 0.080 9 117700861 upstream gene variant A/G snv 0.22 4