Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12683422 0.742 0.240 9 27969442 intron variant C/T snv 5.7E-02 11
rs1408543226
XPA
0.807 0.240 9 97675558 missense variant A/G snv 7.0E-06 6
rs2031920 0.695 0.240 10 133526341 non coding transcript exon variant C/T snv 3.1E-02 20
rs213210 0.742 0.240 6 33208047 upstream gene variant A/C;G snv 11
rs28360071 0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs3734254 0.752 0.240 6 35427233 3 prime UTR variant C/T snv 0.69 14
rs4072037 0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs1045411 0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 18
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs7813 0.689 0.360 17 744946 missense variant G/A;C snv 0.63 22
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1799930 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 17
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25