Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 7
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 6
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 6
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 5
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs9982601 0.851 0.080 21 34226827 intron variant C/T snv 0.15 4
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 3
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 3
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 3
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 3
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 3
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 3
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 3
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 3
rs7395662 0.882 0.080 11 48497341 downstream gene variant A/G snv 0.56 3
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 3
rs1250229 1.000 0.040 2 215439661 upstream gene variant T/C snv 0.77 2