Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2682818 0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1332018 0.882 0.200 1 109740350 5 prime UTR variant G/T snv 0.64 0.66 6
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs2229992
APC
0.827 0.200 5 112827157 stop gained T/C;G snv 0.58 0.47 6
rs6886 0.925 0.160 2 85394936 missense variant T/A;C snv 0.58 4
rs1051992 11 6319476 missense variant A/G snv 4.2E-06; 0.55 0.51 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs228648 0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2303426 0.790 0.080 2 47403411 intron variant C/A;G;T snv 1.9E-05; 0.47 8
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs11651270 0.882 0.240 17 5521757 missense variant T/C snv 0.45 0.47 4