Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9393676 0.925 0.120 6 25936716 intergenic variant G/A snv 0.45 4
rs10001106 0.925 0.120 4 10125817 intergenic variant T/A;C snv 3
rs10003864 0.925 0.120 4 10435767 downstream gene variant T/C snv 0.29 3
rs10009493 0.925 0.120 4 10130423 intergenic variant C/G snv 0.18 3
rs10010656 0.925 0.120 4 10244703 intergenic variant G/C snv 0.30 3
rs1001216 0.925 0.120 4 10167225 non coding transcript exon variant A/G snv 0.15 3
rs1001217 0.925 0.120 4 10167375 non coding transcript exon variant C/A;G snv 3
rs10012288 0.925 0.120 4 10139329 downstream gene variant G/A snv 0.42 3
rs10015494 0.925 0.120 4 10140366 downstream gene variant G/A;C;T snv 3
rs10015872 0.925 0.120 4 10140786 downstream gene variant G/A snv 0.42 3
rs10017305 0.925 0.120 4 10399599 intergenic variant T/C snv 0.26 3
rs10017447 0.925 0.120 4 10173912 regulatory region variant C/A snv 0.67 3
rs10020887 0.925 0.120 4 10139127 downstream gene variant C/A;G snv 3
rs10022911 0.925 0.120 4 10138927 downstream gene variant A/G snv 0.18 3
rs10023177 0.925 0.120 4 10243331 intergenic variant T/A;G snv 3
rs10024152 0.925 0.120 4 10174065 regulatory region variant A/T snv 0.68 3
rs10025456 0.925 0.120 4 10138635 downstream gene variant T/C snv 0.46 3
rs10025702 0.925 0.120 4 10246550 intergenic variant C/G snv 0.20 3
rs10028503 0.925 0.120 4 10140303 downstream gene variant A/G snv 0.42 3
rs10028937 0.925 0.120 4 10140742 downstream gene variant A/G;T snv 3
rs10029208 0.925 0.120 4 10250381 downstream gene variant G/T snv 0.65 3
rs10029818 0.925 0.120 4 10471046 intron variant G/A;C snv 3
rs10030776 0.925 0.120 4 10202851 upstream gene variant C/A;G;T snv 0.66 3
rs10030782 0.925 0.120 4 10202872 upstream gene variant C/T snv 0.68 3
rs10031453 0.925 0.120 4 10141035 downstream gene variant A/C;G snv 3