Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs61776719 0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46 11
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 6
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 6
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 6
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 5
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 4
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 4
rs668948 1.000 0.040 2 21068657 regulatory region variant G/A snv 0.71 4
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 4
rs10106652 1.000 0.040 8 20070649 intergenic variant G/A snv 0.29 3
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 3
rs1250229 1.000 0.040 2 215439661 upstream gene variant T/C snv 0.77 3
rs139401390 0.851 0.120 10 88643382 regulatory region variant A/G snv 1.0E-02 3
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 3