Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs9275141 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 6
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs2523554 0.925 0.080 6 31364052 upstream gene variant C/T snv 0.70 5
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 5
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 5
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs6932542 0.827 0.200 6 32412485 downstream gene variant A/G snv 0.55 5
rs2596560 0.851 0.280 6 31387541 intergenic variant T/C snv 0.22 4
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 4
rs2647050 0.882 0.240 6 32701990 downstream gene variant T/C snv 0.36 4