Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10023050 4 87143279 downstream gene variant A/G snv 0.34 1
rs10023056 4 87143314 downstream gene variant A/G snv 0.19 1
rs1007176 6 164070805 intergenic variant A/G snv 0.55 1
rs1010549 6 164071351 intergenic variant A/C snv 0.50 1
rs10109400 8 42600210 intergenic variant T/C snv 0.66 1
rs1015890 1 47236557 upstream gene variant G/A snv 0.48 1
rs10277087 7 100709915 downstream gene variant G/C snv 0.63 1
rs10434439 4 54536454 intergenic variant G/A;T snv 6.4E-02 1
rs10447387 6 25641872 upstream gene variant A/G snv 0.27 1
rs10484438 6 26308059 intergenic variant T/C snv 0.18 1
rs10487157 7 100616864 downstream gene variant C/G snv 0.16 1
rs10490070 2 60428544 intron variant A/G snv 0.22 1
rs10490071 2 60441755 upstream gene variant G/A snv 0.19 1
rs10503716 8 22009151 downstream gene variant T/C snv 0.13 1
rs10517334 4 54435541 downstream gene variant T/C snv 0.41 1
rs10751500 9 133181719 intergenic variant A/G snv 0.51 1
rs1077181 3 141456114 intron variant C/A snv 0.22 1
rs10786559 10 99549133 intergenic variant G/C;T snv 1
rs1078792 6 30451843 non coding transcript exon variant T/G snv 0.79 1
rs10890472 1 47242440 intergenic variant G/T snv 0.52 1
rs10900450 1 205137110 downstream gene variant C/A;G snv 1
rs10901243 9 133202988 downstream gene variant G/C snv 0.34 1
rs10935459 3 142282445 intergenic variant G/A snv 0.51 1
rs10946795 6 25714511 regulatory region variant A/G snv 7.6E-02 1
rs10946810 6 26287827 upstream gene variant G/A snv 0.27 1