Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7766029 0.851 0.080 6 88137716 downstream gene variant T/C snv 0.51 7
rs10801153 0.925 0.080 1 192794818 intron variant G/A snv 0.27 3
rs2463107 1.000 0.040 12 79699537 intron variant A/C snv 0.36 2
rs2572431 1.000 0.040 8 11247568 downstream gene variant C/G;T snv 2
rs34548976 1.000 0.040 7 31032854 intergenic variant C/T snv 0.39 2
rs4813627 1.000 0.040 20 3074867 downstream gene variant A/G snv 0.51 2
rs11059336 12 127745489 regulatory region variant T/C snv 0.14 1
rs113209956 9 25211195 intergenic variant C/T snv 5.4E-02 1
rs1192553 1 17967858 intergenic variant G/A snv 0.70 1
rs1458103 11 81336231 intron variant A/C snv 0.25 1
rs72711240 4 134774652 intron variant C/T snv 2.2E-02 1
rs9875578 3 13752941 intergenic variant G/A;C snv 1
rs1922242 0.827 0.120 7 87544351 intron variant A/T snv 0.43 8
rs1202184 0.851 0.120 7 87584585 intron variant C/T snv 0.39 7
rs1401663578
ACE
0.882 0.120 17 63483037 missense variant A/G snv 1.4E-05 4
rs2451828 5 7448683 intron variant C/T snv 2.7E-02 1
rs4822492 1.000 0.040 22 24447626 intron variant C/G snv 0.47 4
rs2298383 0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv 11
rs5751876 0.742 0.320 22 24441333 synonymous variant T/C snv 0.54 0.52 16
rs3761422 1.000 0.040 22 24430704 intron variant T/C snv 0.62 4
rs3930965 1.000 0.040 10 4971951 intron variant G/A;C snv 2
rs900418273 0.807 0.120 11 113393764 missense variant A/G snv 8
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs2306073 0.882 0.080 12 27402904 intron variant C/T snv 0.37 4