Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799987 0.763 0.200 3 46370444 intron variant A/G snv 0.49 10
rs652888 0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 10
rs739496 0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 10
rs1834306 0.776 0.200 11 122152479 intron variant A/G snv 0.49 9
rs2284553 0.776 0.240 21 33404389 intron variant A/G snv 0.69 9
rs9261204 0.790 0.200 6 30037466 intron variant A/G snv 0.17 9
rs3130542 0.827 0.160 6 31264334 downstream gene variant A/G snv 0.81 8
rs17401966 0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs9277534 0.790 0.280 6 33087030 3 prime UTR variant A/G snv 0.38 7
rs9275319 0.807 0.200 6 32698518 intergenic variant A/G snv 0.15 6
rs9277378 0.827 0.320 6 33082502 intron variant A/G snv 0.40 5
rs1076064 0.851 0.160 5 149732603 intron variant A/G snv 0.47 4
rs2072906 0.851 0.160 22 43937292 intron variant A/G snv 0.25 0.20 4
rs243327 0.882 0.280 16 11259447 intron variant A/G snv 0.52 4
rs2857261 0.851 0.160 4 141719484 splice region variant A/G snv 0.48 0.49 4
rs2301271 0.882 0.240 6 32757416 intron variant A/G snv 0.60 3
rs3130215 0.882 0.240 6 33107186 intron variant A/G snv 0.69 3
rs421446 0.882 0.280 6 33207006 upstream gene variant A/G snv 0.32 3
rs5000563 0.882 0.240 6 32436358 upstream gene variant A/G snv 0.24 3
rs7773694 0.882 0.280 6 32738557 upstream gene variant A/G snv 0.80 3
rs9276991 0.882 0.240 6 33014071 upstream gene variant A/G snv 6.0E-02 3
rs1042544 0.925 0.200 6 33086680 3 prime UTR variant A/G snv 0.38 2
rs12503843 0.925 0.120 4 83300266 intron variant A/G snv 0.63 2
rs154972 0.925 0.120 6 32932874 downstream gene variant A/G snv 0.35 2
rs2064476 0.925 0.200 6 33105545 intron variant A/G snv 0.37 2