Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1163944538 0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06 73
rs1352010373 0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs1554317002 0.724 0.440 7 39950821 frameshift variant C/- delins 45
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs28937900 0.752 0.160 19 46756276 missense variant C/A;T snv 1.0E-03 37
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs370717845 0.763 0.320 8 43161462 missense variant G/A snv 33
rs63750424 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs104894396 0.672 0.400 13 20189511 stop gained C/T snv 5.8E-04 1.1E-04 28
rs148881970 0.724 0.360 17 42543840 missense variant A/G snv 5.4E-05 1.3E-04 22
rs1555735545 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 22
rs555145190 0.732 0.360 17 42543921 stop gained G/A;C;T snv 4.2E-06 21
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs713041 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs74315408 0.752 0.280 20 4699758 missense variant G/A snv 6.4E-05 4.2E-05 16
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs1556424691
CYTB ; ND6 ; TRNT
0.851 0.200 MT 15923 non coding transcript exon variant A/G snv 13