Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11722228
SLC2A9
0.851 0.160 4 9914117 intron variant C/T snv 0.32 4
rs13129697
SLC2A9
0.925 0.120 4 9925343 intron variant T/G snv 0.39 4
rs16890979
SLC2A9
0.827 0.200 4 9920543 missense variant C/T snv 0.24 0.29 4
rs3114018
ABCG2
0.882 0.160 4 88143429 intron variant A/C snv 0.48 4
rs4698036 0.925 0.120 4 10329670 intergenic variant T/G snv 0.21 4
rs6834555 0.882 0.200 4 10060702 regulatory region variant G/A snv 0.74 4
rs6855911
SLC2A9
0.851 0.200 4 9934286 intron variant A/G snv 0.33 4
rs714873 0.882 0.200 4 10057994 upstream gene variant G/A snv 0.74 4
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 4
rs737267
SLC2A9
0.851 0.240 4 9933120 intron variant G/A;T snv 4
rs7442295
SLC2A9
0.925 0.120 4 9964756 intron variant A/G snv 0.28 4
rs7671266
SLC2A9
0.925 0.120 4 10054752 intron variant T/C snv 0.73 4
rs9291683 0.925 0.120 4 10322536 intergenic variant G/A;C;T snv 4
rs10001106 0.925 0.120 4 10125817 intergenic variant T/A;C snv 3
rs10001964
SLC2A9
0.925 0.120 4 9957651 intron variant C/T snv 0.48 3
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
rs10006397
SLC2A9
0.925 0.120 4 10034516 non coding transcript exon variant C/A snv 0.78 3
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
rs10011796
ABCG2
0.882 0.160 4 88169725 intron variant T/C;G snv 3
rs1001216 0.925 0.120 4 10167225 non coding transcript exon variant A/G snv 0.15 3