Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 7
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 6
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 5
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 5
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 5
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 5
rs12946510 0.851 0.160 17 39756124 downstream gene variant C/T snv 0.37 4
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 4
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 4
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 4
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 4
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 4
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 3
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 3
rs3957148 0.925 0.160 6 32714360 upstream gene variant A/C;G snv 0.10 3
rs6074022 0.851 0.240 20 46111557 TF binding site variant C/G;T snv 3
rs6662618 0.882 0.200 1 92469854 downstream gene variant T/G snv 0.75 3
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 3
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 3
rs9271640 0.925 0.120 6 32624423 upstream gene variant T/C snv 0.76 3
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 2
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2