Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
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
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;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
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs2844513 0.925 0.120 6 31420437 intron variant G/A snv 0.53 6
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 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
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs2428486 0.925 0.120 6 31386327 upstream gene variant T/C snv 0.42 5
rs2844477 0.925 0.120 6 31610995 upstream gene variant T/A;C snv 0.29 5
rs2844529 0.925 0.120 6 31385816 upstream gene variant G/A;T snv 5
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 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
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 5