Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs730881394 0.925 0.320 11 108310222 missense variant C/T snv 4.0E-06 7.0E-06 2
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1383461329 1.000 0.120 12 123389469 missense variant C/T snv 1.4E-05 2
rs773379832 0.925 0.320 9 132297011 missense variant A/G snv 1.2E-05 7.0E-06 2
rs1057519943 0.790 0.160 12 132676598 missense variant G/C;T snv 10
rs1057519944 0.882 0.160 12 132676599 missense variant G/A snv 5
rs1057519958 0.851 0.200 9 134436505 missense variant C/A;T snv 4
rs1800067 0.716 0.320 16 13935176 missense variant G/A snv 5.6E-02 5.3E-02 17
rs750040814
XPC
0.827 0.160 3 14158639 missense variant C/T snv 1.6E-05 5.6E-05 5
rs202003805 0.827 0.120 7 142750561 missense variant C/T snv 9.0E-05 6
rs17107315 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs1057519919 0.851 0.160 2 15942195 missense variant C/T snv 5
rs587782703 0.807 0.160 1 17053947 splice donor variant C/A;T snv 1.2E-05; 4.1E-06 8
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 14
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs1057519936 0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs1057519937 0.776 0.200 3 179234285 missense variant T/C snv 11
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 16
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs764152905 1.000 0.120 16 18854890 missense variant T/A;C snv 8.0E-06; 2.4E-05 1
rs12051350 1.000 0.120 16 18896946 missense variant C/T snv 3.7E-02 1.5E-02 1