Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs587782703 0.807 0.160 1 17053947 splice donor variant C/A;T snv 1.2E-05; 4.1E-06 8
rs1057519919 0.851 0.160 2 15942195 missense variant C/T snv 5
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
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
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 26
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs121913412 0.724 0.280 3 41224633 missense variant A/C;G;T snv 19
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 16
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 14
rs1057519886 0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
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
rs121913413 0.763 0.240 3 41224634 missense variant C/A;T snv 11
rs587778883 0.807 0.200 3 37025648 frameshift variant A/- del 7
rs750040814
XPC
0.827 0.160 3 14158639 missense variant C/T snv 1.6E-05 5.6E-05 5
rs876658923 1.000 0.120 3 36993593 frameshift variant TGAACCG/- delins 3
rs17107315 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs202003805 0.827 0.120 7 142750561 missense variant C/T snv 9.0E-05 6
rs1361241029
PBK
1.000 0.120 8 27828154 start lost T/C snv 2.1E-05 1