Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
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
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs709816
NBN
0.752 0.320 8 89955483 synonymous variant A/G snv 0.47 0.51 10
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs1041983 0.732 0.240 8 18400285 synonymous variant C/T snv 0.34 0.36 15
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs402710 0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38 18
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1056827 0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43