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 60
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
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
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
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 131
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
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 27
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 36
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 97
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 114
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 110
rs3803185 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 19
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 153
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 55
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134