Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10001106 0.925 0.120 4 10125817 intergenic variant T/A;C snv 3
rs10001632
CLNK ; LOC105374482
0.925 0.120 4 10520247 intron variant A/C snv 0.97 2
rs10001964
SLC2A9
0.925 0.120 4 9957651 intron variant C/T snv 0.48 3
rs10002984 0.925 0.120 4 9679109 intron variant T/C snv 0.95 2
rs10003001
SLC2A9
0.925 0.120 4 9982851 intron variant C/T snv 0.21 3
rs10003864 0.925 0.120 4 10435767 downstream gene variant T/C snv 0.29 3
rs10005684 0.925 0.120 4 9625273 intron variant T/A;G snv 2
rs10006397
SLC2A9
0.925 0.120 4 10034516 non coding transcript exon variant C/A snv 0.78 3
rs1000662 0.925 0.120 11 64466347 intergenic variant G/A snv 0.60 2
rs10007469 0.925 0.120 4 9731119 upstream gene variant G/A;C;T snv 2
rs10008035
SLC2A9 ; LOC105374476
0.925 0.120 4 9997711 intron variant G/A;T snv 3
rs10009493 0.925 0.120 4 10130423 intergenic variant C/G snv 0.18 3
rs10009618
ABCG2
0.925 0.120 4 88172856 intron variant C/T snv 0.58 3
rs10010656 0.925 0.120 4 10244703 intergenic variant G/C snv 0.30 3
rs10011206
LOC105374476 ; SLC2A9
0.925 0.120 4 9990331 intron variant C/T snv 0.23 3
rs10011621 0.925 0.120 4 9758615 downstream gene variant A/C snv 0.22 2
rs10011796
ABCG2
0.882 0.160 4 88169725 intron variant T/C;G snv 4
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
rs10012779
SLC2A9
0.925 0.120 4 10036488 intron variant C/T snv 0.15 3
rs10013288
MIR548I2
0.925 0.120 4 9557597 upstream gene variant T/A;G snv 2
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
rs10016022
ZNF518B
0.925 0.120 4 10445282 missense variant A/G;T snv 0.74 3