Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs10031453 0.925 0.120 4 10141035 downstream gene variant A/C;G snv 3
rs10032742 0.925 0.120 4 10277269 intergenic variant A/C;G;T snv 3
rs10033612
SLC2A9
0.925 0.120 4 9983382 intron variant C/T snv 0.20 3
rs10033825
LOC105374482 ; CLNK
0.925 0.120 4 10495168 intron variant C/T snv 0.28 3
rs10033951
SLC2A9
0.925 0.120 4 9777956 intron variant C/T snv 0.35 3
rs10033955 0.925 0.120 4 10176932 intergenic variant T/A;C snv 3
rs10034180
CLNK ; LOC105374482
0.925 0.120 4 10516901 intron variant A/G snv 0.47 3
rs10034405 0.925 0.120 4 10172072 upstream gene variant A/G snv 0.14 3
rs1004327
CLNK ; LOC105374482
0.925 0.120 4 10509859 intron variant C/G;T snv 3
rs1006207
FLRT1 ; MACROD1
11 64082340 intron variant C/G;T snv 1