Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs75316749 0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 17
rs2974935 0.708 0.280 1 155212052 non coding transcript exon variant G/A;C;T snv 17
rs481519 0.708 0.280 3 27285723 intron variant C/A;T snv 17
rs11844632 0.708 0.280 14 68559662 intron variant G/A snv 0.23 17
rs2300206 0.708 0.280 20 34002002 intron variant G/C;T snv 17
rs7725218 0.708 0.280 5 1282299 intron variant G/A snv 0.38 17
rs11168936 0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 16
rs7705526 0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 11
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 11
rs185229225 0.851 0.120 4 13607505 intron variant T/C snv 4
rs7953249 0.882 0.160 12 120965921 splice region variant G/A snv 0.59 4
rs11651755 0.763 0.160 17 37739849 intron variant T/C snv 0.52 4
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs10962692 0.925 0.120 9 16915876 upstream gene variant G/A;C snv 3
rs62274041 0.925 0.120 3 156717851 upstream gene variant G/A;T snv 3
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 3
rs8170 0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 3
rs711830 0.882 0.120 2 176172583 3 prime UTR variant A/C;G;T snv 0.76 3
rs6755777 0.882 0.120 2 176178498 non coding transcript exon variant T/A;G snv 3
rs7405776 0.807 0.120 17 37733029 intron variant G/A;C snv 3
rs2494938 0.752 0.240 6 40568389 intron variant G/A snv 0.51 3
rs183211 0.882 0.160 17 46710944 intron variant G/A snv 0.28 0.30 3
rs2227564 0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 3