Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 7
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 7
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 7
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 7
rs1329568 0.882 0.120 9 37037979 upstream gene variant T/A;G snv 6
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 6
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 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
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 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
rs9461799 0.807 0.360 6 32721752 downstream gene variant T/C snv 0.37 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
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 5
rs2844477 0.925 0.120 6 31610995 upstream gene variant T/A;C snv 0.29 5
rs2844479 0.925 0.200 6 31605179 intergenic variant A/C snv 0.34 5
rs2844529 0.925 0.120 6 31385816 upstream gene variant G/A;T snv 5
rs2856683 0.827 0.320 6 32687441 regulatory region variant T/A;C;G snv 0.25 5
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs3129859 0.827 0.320 6 32433162 intergenic variant G/C;T snv 5