Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs11953630 5 158418394 intergenic variant C/A;T snv 6
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs35444 12 115114632 intergenic variant A/G snv 0.38 6
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 6
rs7753826 0.925 0.120 6 26042011 upstream gene variant T/A;C snv 6
rs9292468 5 32818967 intergenic variant T/A;C snv 6
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs10184428 2 164155317 intron variant C/A;G snv 5
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs1173766 5 32804422 intergenic variant T/C snv 0.57 5
rs13082711 3 27496418 intergenic variant T/C snv 0.16 5
rs13209747 6 126794309 intron variant C/G;T snv 0.36 5