Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs130058 0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs751416416 0.882 0.120 8 53250920 missense variant C/A;T snv 8.3E-06; 4.1E-06 5