Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs2949506 0.851 0.160 18 30217168 intergenic variant C/T snv 0.14 5
rs200538373 0.925 0.120 19 1061893 splice region variant G/A;C snv 2.5E-03 2
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs201564694 0.882 0.120 1 159588626 missense variant T/C snv 3
rs1217777010 1.000 0.040 11 116836182 missense variant C/T snv 4.0E-06 1
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs371425292
APP
0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06 10
rs63750847
APP
0.790 0.120 21 25897620 missense variant C/T snv 4.5E-04 3.0E-04 8
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs950592627
APP
0.827 0.200 21 26090015 missense variant G/C snv 7.0E-06 5
rs529782627
APP
0.882 0.120 21 26112051 missense variant C/A snv 4.0E-06 7.0E-06 3
rs763852444
APP
0.882 0.120 21 26112127 missense variant G/C snv 4.0E-06 3
rs10097505
ARC
0.925 0.120 8 142612823 3 prime UTR variant G/A snv 0.47 2
rs73956431 0.827 0.120 18 31699870 regulatory region variant C/T snv 8.4E-02 6
rs970866 0.851 0.160 18 31681955 intron variant C/T snv 0.89 4
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs140226130 0.790 0.200 18 33336845 intron variant -/CTTTTTGCT delins 7.8E-02 8
rs2279590
CLU
0.851 0.200 8 27598736 non coding transcript exon variant T/C snv 0.69 5
rs7982
CLU
1.000 0.040 8 27604964 missense variant A/C;G snv 0.64 0.60 1
rs9331888 0.827 0.200 8 27611345 5 prime UTR variant C/G snv 0.35 0.28 5
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv 8
rs28939068 0.790 0.200 20 23635330 missense variant A/T snv 9