Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs324981 0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs821616 0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs1126647 0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs1800044 0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03 8
rs1059004 0.925 0.040 21 33028155 3 prime UTR variant C/A snv 0.41 4
rs1555103646 1.000 0.040 12 13569964 missense variant C/A snv 4
rs10509125 10 60167108 intron variant C/A snv 0.56 2
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs6994992 0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs80338758 0.790 0.400 X 71127367 missense variant C/A;T snv 12
rs27072 0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs121918805 0.925 0.080 2 166002660 missense variant C/A;T snv 2.0E-05 4
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs886041097 0.882 0.160 4 139386152 stop gained C/G snv 9
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs1133503 1.000 0.040 6 95606712 3 prime UTR variant C/G;T snv 4
rs1799920 5 63961656 missense variant C/G;T snv 3.2E-04 2
rs35369693 1 206116696 missense variant C/G;T snv 4.3E-02 2
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237