Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1367644026
KRT5
0.925 0.080 12 52520259 missense variant C/A;T snv 4.0E-06 5
rs113994088
ALK
0.925 0.080 2 29222584 missense variant C/G snv 4
rs1057519888
EGFR
0.925 0.080 7 55143386 missense variant A/G snv 3
rs139236063
EGFR
0.925 0.080 7 55165350 missense variant G/C;T snv 3
rs113994087
ALK
0.827 0.120 2 29209798 missense variant C/A;T snv 12
rs371409680
TP53
0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 10
rs1057519906
IDH2
0.882 0.120 15 90088607 missense variant T/A;C snv 8
rs1872328
ACYP2
0.827 0.120 2 54168122 intron variant G/A snv 7.3E-02 6
rs1057519757
PIK3R1
0.882 0.120 5 68293310 missense variant G/A;C snv 5
rs1057519841
PIK3R1
0.925 0.120 5 68295269 missense variant A/G snv 5
rs113994089
ALK
0.925 0.120 2 29220776 missense variant C/G;T snv 4
rs80359183
BRCA2
0.882 0.120 13 32380096 stop gained T/A;C snv 4
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs1057519902
H3-3A
0.742 0.160 1 226064451 missense variant G/C snv 16
rs397516813
RAF1
0.925 0.160 3 12599717 missense variant C/G snv 3
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs1057519940
PIK3CA
0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519936
PIK3CA
0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs1057519937
PIK3CA
0.776 0.200 3 179234285 missense variant T/C snv 11
rs1057519926
PIK3CA
0.776 0.200 3 179210293 missense variant A/T snv 10
rs11568821
LOC105373977 ; PDCD1
0.827 0.200 2 241851760 intron variant C/G;T snv 10
rs1052576
CASP9
0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs1800435
ALAD
0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 7
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 19