Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10878232 1.000 0.080 12 65128867 intergenic variant T/A;C;G snv 1
rs11674251 1.000 0.080 2 20016748 upstream gene variant T/C snv 0.18 1
rs12000445 1.000 0.080 9 23426273 intron variant A/G snv 0.18 1
rs1209950 1.000 0.080 21 38801604 upstream gene variant C/T snv 0.30 1
rs1414493 1.000 0.080 1 241523216 upstream gene variant A/G snv 0.62 1
rs1957860 1.000 0.080 14 53962637 upstream gene variant C/T snv 0.51 1
rs4743325 1.000 0.080 9 99087445 intergenic variant G/T snv 0.24 1
rs6122390 1.000 0.080 20 63173912 intron variant C/T snv 0.27 1
rs7629386 1.000 0.080 3 40925416 regulatory region variant C/T snv 0.30 1
rs9660710 1.000 0.080 1 1163962 upstream gene variant A/C;T snv 1
rs969088 1.000 0.080 5 26389153 intron variant G/C snv 9.9E-02 1
rs9909179 1.000 0.080 17 13140986 regulatory region variant T/C snv 0.37 1
rs750443908 1.000 0.080 10 50859904 missense variant C/A;T snv 6.0E-05; 8.0E-06 1
rs2725264 1.000 0.080 4 88104957 intron variant C/T snv 0.70 1
rs4148149 1.000 0.080 4 88141133 intron variant T/G snv 0.42 1
rs768122549 1.000 0.080 20 34260386 synonymous variant C/G;T snv 4.0E-06 1
rs754845817 1.000 0.080 12 111790494 missense variant G/A snv 1.6E-05 1.4E-05 1
rs550608288
ALK
1.000 0.080 2 29717646 missense variant T/C snv 5.2E-05 1
rs958335893
ALK
1.000 0.080 2 29193478 missense variant C/T snv 1
rs919968 1.000 0.080 15 79205004 intron variant T/A;G snv 1
rs41997 1.000 0.080 7 118351841 intron variant A/G snv 0.27 1
rs228590
ATM
1.000 0.080 11 108225414 5 prime UTR variant A/G snv 0.52 1
rs170548 1.000 0.080 11 108364109 intron variant A/C;T snv 1
rs9526814 1.000 0.080 13 51965390 intron variant T/G snv 0.35 1
rs17878624 1.000 0.080 17 78224418 3 prime UTR variant G/A snv 5.0E-04 1