Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7040869 1.000 0.080 9 99072866 downstream gene variant G/A snv 0.11 2
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs201661522 1.000 0.080 7 87539293 missense variant A/G snv 6.4E-05 1.0E-04 2
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs3740066 0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs717620 0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
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
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs751306825
ALK
0.925 0.080 2 29220759 missense variant G/A;T snv 4.0E-06 4
rs863225283
ALK
0.925 0.080 2 29213993 missense variant A/C snv 4
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs2245214 0.827 0.240 6 106214866 intron variant C/G snv 0.42 6
rs2227928
ATR
0.851 0.200 3 142562770 missense variant A/G snv 0.55 0.63 6
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
rs1564483 1.000 0.080 18 63127421 3 prime UTR variant C/T snv 0.22 4
rs2279115 0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv 18
rs1042489 0.851 0.160 17 78224125 3 prime UTR variant T/C snv 0.40 5
rs8073069 0.807 0.200 17 78213692 upstream gene variant G/C snv 0.33 7
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52