Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2516460 1.000 0.080 6 31450923 intron variant T/A;C;G snv 0.54 1
rs2523485 1.000 0.080 6 31383258 upstream gene variant T/C snv 0.87 1
rs2523638 1.000 0.080 6 31376496 upstream gene variant T/C snv 0.45 1
rs2530709 1.000 0.080 6 30972792 intergenic variant G/A;C;T snv 1
rs2530710 1.000 0.080 6 30972610 intergenic variant T/C snv 0.86 1
rs2596517 1.000 0.080 6 31392318 downstream gene variant G/A snv 0.85 1
rs2621382 1.000 0.080 6 32792668 intergenic variant G/C;T snv 1
rs2736177 1.000 0.080 6 31618317 upstream gene variant C/T snv 0.91 1
rs2744148 1.000 0.080 16 1023552 intergenic variant A/G snv 0.15 1
rs2844558 1.000 0.080 6 31372656 intron variant C/T snv 0.46 1
rs2857129 1.000 0.080 6 32808846 downstream gene variant A/T snv 0.67 1
rs2857136 1.000 0.080 6 32807909 downstream gene variant A/G snv 0.67 1
rs2857154 1.000 0.080 6 32794839 intergenic variant A/G snv 0.67 1
rs2857212 1.000 0.080 6 32772634 intergenic variant A/G;T snv 1
rs2920001 1.000 0.080 18 31209762 intergenic variant T/C snv 0.20 1
rs3016013 1.000 0.080 6 31383465 upstream gene variant G/A snv 0.71 1
rs3095238 1.000 0.080 6 31193433 upstream gene variant T/G snv 0.88 1
rs3095250 1.000 0.080 6 31240563 intergenic variant C/T snv 0.58 1
rs3095345 1.000 0.080 6 30854636 intergenic variant C/T snv 0.84 1
rs3099848 1.000 0.080 6 31383665 upstream gene variant A/G;T snv 1
rs3129305 1.000 0.080 6 32991403 intergenic variant G/C snv 0.93 1
rs3129889 1.000 0.080 6 32445768 downstream gene variant G/A;T snv 1
rs3130532 1.000 0.080 6 31240676 intergenic variant A/G snv 0.88 1
rs3130534 1.000 0.080 6 31241268 intergenic variant G/A snv 0.54 1
rs3130952 1.000 0.080 6 31210138 intergenic variant G/A snv 0.88 1