Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs149617956 0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 32
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44