Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3129932 0.925 0.160 6 32368350 intron variant G/C snv 0.76 3
rs3130320 0.851 0.160 6 32255481 intron variant T/C snv 0.68 5
rs3135342 0.925 0.160 6 32428838 intergenic variant G/T snv 0.24 2
rs3135377 0.925 0.160 6 32417622 regulatory region variant A/G snv 0.80 2
rs3135392 0.925 0.160 6 32441465 intron variant C/A snv 0.38 2
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs404890 0.925 0.160 6 32231090 intergenic variant C/A snv 0.35 2
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 5
rs437179 0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs4750316 0.882 0.160 10 6351298 non coding transcript exon variant C/G;T snv 5
rs486416 0.925 0.160 6 31888293 intron variant G/A snv 0.77 0.76 2
rs5029937 0.882 0.160 6 137874014 intron variant G/T snv 0.13 4
rs535586 0.882 0.160 6 31892560 splice region variant T/A;C snv 0.77 3
rs644827 0.882 0.160 6 31870664 missense variant T/C snv 0.60 0.60 3
rs659445 0.882 0.160 6 31896527 intron variant G/A;C snv 0.77 0.76 3
rs660550 0.882 0.160 6 31869500 intron variant C/A;G snv 0.60 3
rs6684865 0.925 0.160 1 2614790 intron variant G/A snv 0.40 2
rs682626 0.925 0.160 19 6774058 intron variant G/A;T snv 2
rs6859219 0.925 0.160 5 56142753 intron variant C/A snv 0.20 4
rs6936204 0.925 0.160 6 32249315 intergenic variant T/C snv 0.70 3
rs793108 0.925 0.160 10 31126177 intron variant C/T snv 0.40 2
rs874040 0.925 0.160 4 26106575 downstream gene variant G/C snv 0.29 4
rs9267873 0.925 0.160 6 32231575 intergenic variant C/G;T snv 2
rs9268429 0.925 0.160 6 32377275 intron variant A/G snv 0.24 2
rs9268832 0.882 0.160 6 32460012 non coding transcript exon variant T/C snv 0.61 0.59 4