Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10806425 0.851 0.280 6 90216893 intron variant C/A snv 0.33 6
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs11712165 0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs1250552 0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs12928822 0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs13003464 0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs13010713 0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs13098911 0.882 0.200 3 46193709 intron variant C/G;T snv 5
rs13151961 0.827 0.200 4 122194347 intron variant A/G snv 0.11 7
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs17035378 0.882 0.200 2 68371823 intron variant T/A;C snv 5
rs17810546 0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 7
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs2816316 0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs296547 0.882 0.200 1 200923009 intron variant T/C snv 0.53 5
rs41423247 0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs4646536 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 14
rs4675374 0.882 0.200 2 203937855 intron variant T/C snv 0.65 5
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs6927172 0.851 0.120 6 137681038 intron variant C/A;G;T snv 5
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7