Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1454694 0.827 0.080 4 181276794 intergenic variant T/C snv 0.20 5
rs9295740 0.827 0.120 6 27721723 intergenic variant G/A snv 0.27 5
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs4957014 0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs778561687 0.851 0.080 19 40235953 missense variant C/A;T snv 4.0E-06; 4.0E-06 4
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 8
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs2307486 0.790 0.240 14 20456045 missense variant A/G snv 7.4E-03 2.1E-03 7
rs763375936 0.827 0.160 3 112532749 missense variant C/T snv 8.3E-06 7.0E-06 5
rs772776695 0.827 0.160 3 112548576 missense variant T/A snv 4.0E-06 5
rs751688663 0.807 0.280 3 11340656 missense variant G/A snv 4.0E-06 7
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs9535826 0.851 0.080 13 51991990 intron variant T/C;G snv 4
rs767935771
AXL
0.827 0.080 19 41259690 missense variant T/C snv 1.6E-05 5.6E-05 6
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490