Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs3021094 0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 8
rs3790622 0.882 0.320 1 206771818 intron variant G/A snv 1.5E-03 3