Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1019535182
XPA
1.000 0.160 9 97684921 splice donor variant A/G snv 1
rs104894131
XPA
1.000 0.160 9 97689600 missense variant C/A;T snv 4.0E-06; 4.0E-06 1
rs104894134
XPA
1.000 0.160 9 97689575 stop gained A/G;T snv 4.0E-06 1
rs1057519018
XPA
1.000 0.160 9 97684947 frameshift variant CT/- delins 4.0E-06 1
rs1240801740
XPA
1.000 0.160 9 97687191 stop gained CA/- delins 4.0E-06 7.0E-06 1
rs1253496792
XPA
1.000 0.160 9 97697291 start lost A/G snv 1
rs1326841833
XPA
1.000 0.160 9 97687118 frameshift variant -/T delins 4.0E-06 1
rs144725456
XPA
1.000 0.160 9 97675530 missense variant T/C snv 1.3E-04 7.7E-05 1
rs1554699296
XPA
1.000 0.160 9 97675528 frameshift variant -/A delins 1
rs1554699334
XPA
1.000 0.160 9 97675584 stop gained A/T snv 1
rs1554701129
XPA
1.000 0.160 9 97684964 frameshift variant -/G delins 1
rs1554701139
XPA
1.000 0.160 9 97684994 frameshift variant CT/- delins 1
rs1554701144
XPA
1.000 0.160 9 97685023 frameshift variant AA/- del 1
rs1554701152
XPA
1.000 0.160 9 97685033 frameshift variant T/- delins 1
rs1554701478
XPA
1.000 0.160 9 97687094 splice donor variant A/T snv 1
rs1554701481
XPA
1.000 0.160 9 97687095 splice donor variant C/T snv 1
rs1554701488
XPA
1.000 0.160 9 97687103 frameshift variant T/- delins 1
rs1554701520
XPA
1.000 0.160 9 97687178 frameshift variant -/T delins 1
rs1554701532
XPA
1.000 0.160 9 97687200 stop gained T/A snv 1
rs1554701540
XPA
1.000 0.160 9 97687222 frameshift variant CT/- delins 1
rs1554701563
XPA
1.000 0.160 9 97687260 frameshift variant C/- del 1
rs1554701931
XPA
1.000 0.160 9 97689533 splice donor variant C/T snv 1
rs1554702597
XPA
1.000 0.160 9 97693643 splice donor variant TTACCT/- delins 1
rs1554702608
XPA
1.000 0.160 9 97693697 stop gained C/A snv 1
rs1554702629
XPA
1.000 0.160 9 97693735 frameshift variant G/- delins 1