Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188