Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs3129943 0.851 0.240 6 32370918 intron variant A/G snv 0.26 4
rs10036748 0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs5743836 0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
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
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs721917 0.752 0.360 10 79946568 missense variant A/G snv 0.47 0.42 14
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs12150220 0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14
rs2670660 0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2855812 0.790 0.360 6 31504943 intron variant G/T snv 0.23 13