Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
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
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105