Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2585428 0.763 0.200 20 54170358 intron variant C/T snv 0.46 11
rs74315364 0.732 0.200 1 182586014 stop gained C/A snv 3.6E-03; 4.0E-06 3.3E-03 13
rs4988483 0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11
rs80359584 0.807 0.280 13 32340757 frameshift variant CTTAA/- delins 4.2E-06 1.4E-05 8
rs887303970 0.776 0.280 4 24799565 missense variant C/T snv 8.8E-06 7.0E-06 10
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs2066827 0.695 0.320 12 12718165 missense variant T/A;C;G snv 1.6E-04; 1.6E-05; 0.26 21
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs1800440 0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs2308321 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37