Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1130233 0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs12683422 0.742 0.240 9 27969442 intron variant C/T snv 5.7E-02 11
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs2031920 0.695 0.240 10 133526341 non coding transcript exon variant C/T snv 3.1E-02 20
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs11671784 0.790 0.240 19 13836482 non coding transcript exon variant G/A snv 1.2E-02 1.2E-02 9
rs125701 0.790 0.160 3 9748794 upstream gene variant G/A snv 0.13 7
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2839698 0.662 0.520 11 1997623 non coding transcript exon variant G/A snv 0.41 25
rs2976392
JRK ; PSCA
0.724 0.240 8 142681514 3 prime UTR variant G/A snv 0.46 0.45 15
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs3807987 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17