Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs8177400
TIRAP
0.882 0.160 11 126292695 missense variant G/A;C;T snv 2.8E-03; 1.2E-05 4
rs138228187
TIRAP
0.925 0.120 11 126292650 missense variant C/T snv 4.0E-05 1.4E-05 3
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs61756766
TNFRSF13C
0.776 0.320 22 41925447 missense variant G/A snv 5.7E-03 5.7E-03 9
rs867830180
TNFRSF6B ; RTEL1 ; RTEL1-TNFRSF6B
0.925 0.120 20 63695147 missense variant G/A;T snv 3
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs1555525126
TP53
0.925 0.120 17 7673749 missense variant T/C snv 3
rs1351687973
TP73
0.925 0.120 1 3731497 missense variant G/A snv 1.6E-05 3
rs535311760
TP73
0.925 0.120 1 3730979 missense variant G/A snv 1.2E-05; 8.2E-06 3
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
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205