Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
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
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs112735431 0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18