Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs2839698 0.662 0.520 11 1997623 non coding transcript exon variant G/A snv 0.41 25
rs1141718 0.724 0.280 6 159688224 missense variant A/G snv 15
rs25648 0.742 0.320 6 43771240 synonymous variant C/G;T snv 8.5E-06; 0.16 11