Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11254413 0.851 0.120 10 17162188 missense variant G/A snv 0.41 0.44 4
rs207454
XDH
0.851 0.120 2 31344766 intron variant T/G snv 0.11 0.16 4
rs2494752 0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs2736109 0.851 0.120 5 1296644 upstream gene variant C/T snv 0.32 4
rs2808668
XPA
0.851 0.120 9 97690153 intron variant C/G;T snv 7
rs353639 0.851 0.120 11 35162817 intron variant T/G snv 0.32 5
rs752681512 0.851 0.120 5 7897088 missense variant A/G snv 2.0E-05 4
rs753535070 0.851 0.120 1 155187350 missense variant T/C snv 8.0E-06 5
rs7972 0.851 0.120 14 77326894 missense variant G/A snv 7.0E-02 7.0E-02 4
rs80358829 0.827 0.120 13 32340327 missense variant C/T snv 6
rs1562430 0.807 0.160 8 127375606 intron variant T/C snv 0.41 6
rs2240688 0.790 0.160 4 15968726 3 prime UTR variant T/G snv 0.22 7
rs5277 0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 9
rs828907 0.827 0.160 2 216108009 intron variant G/T snv 0.37 6
rs113593938 0.790 0.200 21 44250907 missense variant C/T snv 3.5E-03 7
rs1801200 0.790 0.200 17 39723335 missense variant A/G;T snv 7
rs2293303 0.827 0.200 3 41239336 synonymous variant C/T snv 3.2E-02 1.2E-02 7
rs3747093 0.732 0.200 22 21630090 upstream gene variant G/A snv 0.32 16
rs6498486 0.776 0.200 16 13919809 upstream gene variant A/C snv 0.27 8
rs6713088 0.763 0.200 2 54118332 intron variant C/G snv 0.48 9
rs6917
PHB
0.790 0.200 17 49404181 3 prime UTR variant G/A snv 0.16 7
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs10511729 0.742 0.240 9 23557229 intron variant T/G snv 0.35 11
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs12683422 0.742 0.240 9 27969442 intron variant C/T snv 5.7E-02 11