Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs238406 0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs12587 0.827 0.200 12 25205894 3 prime UTR variant T/G snv 0.49 5
rs863225285
ALK
0.851 0.080 2 29209789 missense variant T/G snv 5
rs10162417 1.000 0.040 14 22460708 intron variant T/G snv 0.15 1
rs2191311 1.000 0.040 7 38295919 non coding transcript exon variant T/G snv 0.33 1
rs3811215 1.000 0.040 14 22485789 upstream gene variant T/G snv 0.80 1
rs3811244 1.000 0.040 14 22391078 intron variant T/G snv 0.35 1
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs1800975
XPA
0.701 0.360 9 97697296 5 prime UTR variant T/C;G snv 0.63; 4.5E-06; 4.5E-06 19
rs1475170339 0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs653765 0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10
rs79977247
TTR
0.776 0.200 18 31592975 missense variant T/C;G snv 9
rs121912452 0.807 0.120 21 31667271 missense variant T/C;G snv 4.0E-06 6
rs4712653 0.882 0.080 6 22125735 intron variant T/C;G snv 3
rs765771575
MET
0.882 0.080 7 116782017 missense variant T/C;G snv 4.0E-06; 4.0E-06 3
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs34330 0.724 0.280 12 12717761 5 prime UTR variant T/C snv 0.70 15
rs3136817 0.732 0.280 14 20456275 intron variant T/C snv 0.23 12
rs391957 0.763 0.240 9 125241745 non coding transcript exon variant T/C snv 0.72 10
rs35870237 0.763 0.120 12 40340404 missense variant T/C snv 9