Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799768 0.807 0.360 7 101126425 upstream gene variant -/A;C ins 6
rs1524668 0.851 0.160 2 9557243 upstream gene variant A/C snv 0.64 4
rs2664581
PI3
0.882 0.120 20 45175881 missense variant A/C snv 0.16 0.16 3
rs2808530 0.925 0.080 9 98576823 intron variant A/C snv 0.12 2
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs6958571 0.925 0.080 7 30446094 intron variant A/C;G snv 1.2E-05; 0.25; 5.3E-05 3
rs595209 0.925 0.080 11 126292326 intron variant A/C;G snv 2
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1764390 0.882 0.160 1 34794360 missense variant A/C;G;T snv 0.61 0.69 3
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs34557412 0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 15
rs867186 0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 15
rs4648068 0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs12692386 0.827 0.160 2 9555777 5 prime UTR variant A/G snv 0.72 5
rs12048215 0.882 0.160 1 247421289 intron variant A/G snv 0.11 3
rs4684846 0.882 0.080 3 12297350 intron variant A/G snv 0.28 3
rs773829498 0.882 0.080 7 101130457 missense variant A/G snv 4.0E-06 3
rs11666254 0.925 0.080 19 51759909 intron variant A/G snv 0.28 2