Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 97
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs1799796 0.790 0.240 14 103699590 intron variant T/A;C snv 0.31 7
rs200182588 0.827 0.160 9 104094409 5 prime UTR variant -/GC ins 7.0E-06 6
rs156113 0.925 0.080 6 104369868 intergenic variant A/T snv 0.96 2
rs2494732 0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs3730358 0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs636291 0.925 0.080 1 10496040 intron variant G/A snv 0.55 2
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 5
rs1221877686 0.925 0.080 4 105234193 missense variant G/A snv 2
rs12315175 0.925 0.080 12 107105494 intron variant T/C snv 0.18 2
rs817826 0.925 0.080 9 107394019 intergenic variant C/T snv 0.81 2
rs4988483 0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11
rs197056 0.925 0.080 16 1081695 upstream gene variant A/C;G snv 2
rs197057 0.925 0.080 16 1082015 upstream gene variant C/G snv 0.53 2
rs1800057
ATM
0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 8
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 37
rs2278911 0.925 0.080 3 108579413 missense variant C/T snv 0.16 0.12 2
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs1046040 0.925 0.080 19 1095515 upstream gene variant G/A snv 0.21 2
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs7483 0.742 0.320 1 109737079 missense variant C/T snv 4.0E-06; 0.35 0.26 11