Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs3819025 0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02 11
rs3869109 0.851 0.160 6 31216419 intergenic variant A/G;T snv 5
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs6136 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17