Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1467465 0.827 0.160 1 27884892 non coding transcript exon variant A/G snv 0.61 7
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs5013329 0.827 0.160 1 46349419 intron variant C/T snv 0.23 6
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs851797 0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs2227982 0.677 0.480 2 241851281 missense variant G/A snv 9.2E-02 4.3E-02 24
rs267607911 0.851 0.200 2 47403192 start lost A/C;G;T snv 5.1E-05; 1.4E-05 8
rs28997576 0.776 0.160 2 214752454 missense variant C/G;T snv 1.5E-02 11
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 43
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 62
rs17251221 0.724 0.360 3 122274400 intron variant A/G snv 0.11 16
rs1799977 0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60