Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs752855469
MTR
1.000 0.040 1 236803460 missense variant A/G snv 4.0E-06 1
rs767197560 1.000 0.040 8 32760357 missense variant C/G snv 4.0E-06 1.4E-05 1
rs770029196 1.000 0.040 8 32749563 missense variant C/G snv 4.0E-06 1
rs773016917 1.000 0.040 14 18967839 synonymous variant C/G;T snv 1
rs10033029 1.000 0.040 4 86764643 missense variant T/C;G snv 9.4E-06; 8.0E-02 1
rs28903095 1.000 0.040 4 39321353 missense variant C/T snv 1.9E-04 1.0E-04 1
rs768388223 1.000 0.040 14 94614795 synonymous variant C/T snv 4.0E-06 1
rs1049430 1.000 0.040 9 17796670 3 prime UTR variant T/G snv 0.62 1
rs148573932 1.000 0.040 12 57232791 missense variant A/G snv 2.8E-05 7.0E-05 1
rs12452890 1.000 0.040 17 78134989 synonymous variant G/A snv 0.54 0.58 1
rs201613442 1.000 0.040 1 74540276 missense variant G/A snv 4.0E-06 1
rs757503234
XPC
1.000 0.040 3 14158838 missense variant T/C snv 1
rs180127 0.925 0.040 17 69923642 intergenic variant G/A;C snv 2
rs1972597 1.000 0.040 17 77598082 intron variant T/C snv 0.31 2
rs3862188 1.000 0.040 1 247702471 intron variant T/C snv 0.44 2
rs26537 0.925 0.080 5 115841317 3 prime UTR variant T/C;G snv 2
rs4150351 0.925 0.160 13 102870617 intron variant A/C;T snv 2
rs2012775 1.000 0.040 9 115141569 intron variant T/C snv 0.30 2
rs3218123 0.925 0.120 1 23531364 upstream gene variant C/A;G snv 2
rs754426793 0.925 0.080 7 55181395 missense variant G/A snv 1.2E-05 1.4E-05 2
rs758434928 0.925 0.160 11 65570895 missense variant C/T snv 4.8E-05 1.4E-05 2
rs1057519905 0.925 0.080 6 27872234 missense variant T/C snv 2
rs544899118 0.925 0.160 14 94115873 missense variant T/C snv 4.4E-06 7.0E-06 2
rs1360602468 0.925 0.080 14 103698904 missense variant G/C;T snv 2
rs121909237 1.000 0.040 10 87933121 missense variant C/G snv 2