Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs28929495 0.807 0.120 7 55174014 missense variant G/A;C;T snv 9
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs1179251 0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs35301225 0.882 0.080 1 9151743 mature miRNA variant C/A;T snv 5