Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10016702
ZNF518B
0.925 0.120 4 10446016 missense variant A/G;T snv 0.12; 4.0E-06 2
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
rs10017674
SLC2A9
0.925 0.120 4 9965429 intron variant T/C snv 0.49 3
rs10018204
SLC2A9
0.925 0.120 4 9962946 intron variant C/T snv 0.49 3
rs10020053
SLC2A9
0.925 0.120 4 9820024 intron variant T/C snv 0.54 2
rs10020887 0.925 0.120 4 10139127 downstream gene variant C/A;G snv 3
rs10022012 0.925 0.120 4 9691558 intron variant A/T snv 0.34 2
rs10022499
LOC105374476 ; SLC2A9
0.925 0.120 4 10004913 intron variant C/A snv 0.72 3
rs10022911 0.925 0.120 4 10138927 downstream gene variant A/G snv 0.18 3
rs10023068
LOC105374476 ; SLC2A9
0.925 0.120 4 10003208 intron variant A/G snv 0.72 3
rs10023177 0.925 0.120 4 10243331 intergenic variant T/A;G snv 3
rs10023457
ABCG2
0.925 0.120 4 88213552 intron variant T/A snv 0.38 2
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
rs10029311
SLC2A9
0.925 0.120 4 10039510 intron variant T/C snv 0.14 3
rs10029818 0.925 0.120 4 10471046 intron variant G/A;C snv 3
rs10030521
CLNK
0.925 0.120 4 10534793 intron variant C/G;T 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
rs10031303
SLC2A9
0.925 0.120 4 9840066 intron variant A/T snv 0.54 3