Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs208294 0.790 0.320 12 121162450 missense variant T/A;C;G snv 0.51 9
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs4644 0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
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
rs1058587 0.882 0.200 19 18388612 missense variant C/G;T snv 0.24; 9.1E-06 4
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
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
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105