Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs10865710 0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs3812316 0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02 14
rs7566605 0.752 0.320 2 118078449 regulatory region variant C/G snv 0.70 11
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs2297508 0.790 0.240 17 17812003 synonymous variant C/G;T snv 0.50; 7.5E-05 8
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs749710704 0.790 0.160 5 79119289 missense variant C/G;T snv 4.0E-06; 4.0E-06 7
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs1181860747 0.776 0.240 19 7122961 missense variant C/T snv 10
rs118204060
LPL
0.807 0.160 8 19954279 missense variant C/T snv 4.0E-05 1.4E-05 9