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
rs1329568 0.882 0.120 9 37037979 upstream gene variant T/A;G snv 6
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 6
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 5
rs9880772 0.827 0.240 3 27736288 intergenic variant G/A snv 0.59 5
rs112846137 0.851 0.160 3 160595133 intergenic variant G/T snv 5.3E-02 4
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 4
rs193107685 0.851 0.160 7 74123572 downstream gene variant T/C snv 1.0E-02 4
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 4
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 4
rs58721818 0.851 0.160 6 137922602 regulatory region variant C/G;T snv 4
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 4
rs744600 0.851 0.160 2 190700031 intron variant G/T snv 0.60 4
rs7929541 0.851 0.160 11 633689 upstream gene variant T/C snv 0.34 4
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 4
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 3
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 3
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 3