Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
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
rs1862513 0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1800450 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs8193037 0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs11203203 0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs2292596 0.827 0.240 5 422840 missense variant C/G;T snv 0.38; 4.0E-06 7
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82