Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs6651252 0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs13132308 0.807 0.160 4 122629959 intron variant A/G snv 0.10 6
rs3748816 0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 2