Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61755320 0.716 0.520 16 89546737 missense variant C/T snv 2.9E-03 3.5E-03 41
rs1564045331
XPA
0.716 0.320 9 97687208 inframe deletion ATTCTT/- delins 35
rs778543124
XPA
0.716 0.320 9 97675476 frameshift variant AGTCTTACGGTACA/- delins 6.8E-05 6.3E-05 35
rs113994095 0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 31
rs375817528 0.776 0.160 11 65206824 splice region variant G/A snv 1.2E-04 1.2E-04 25
rs1554768245 0.807 0.160 6 152472395 frameshift variant C/- delins 16