Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913361
BRAF
0.807 0.280 7 140753349 missense variant C/A;G;T snv 7
rs121913468
ERBB2
0.827 0.160 17 39724008 missense variant G/A;C;T snv 7
rs1057519920
NFE2L2
0.790 0.160 2 177234232 missense variant C/A;G;T snv 7
rs1057519922
NFE2L2
0.790 0.200 2 177234082 missense variant C/G;T snv 7
rs80359601
BRCA2
0.807 0.360 13 32340890 frameshift variant -/A;NNNNNNNN ins 4.1E-06 8
rs1057519881
CDKN2A
0.776 0.240 9 21971111 missense variant T/C snv 8
rs1057519890
ERBB2
0.807 0.200 17 39723966 missense variant T/A snv 8
rs759610249
FBXW7
0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs1057519928
PIK3CA
0.807 0.200 3 179221147 missense variant A/C snv 8
rs786201419
TP53
0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs9642880
CASC11
0.776 0.240 8 127705823 intron variant G/A;T snv 9
rs121913385
CDKN2A
0.763 0.240 9 21971112 missense variant G/A;C snv 9
rs34968276
CDKN2A
0.776 0.240 9 21971110 stop gained G/A;C;T snv 9
rs1057519893
ERBB3
0.790 0.160 12 56085070 missense variant G/A;T snv 9
rs786203071
TP53
0.776 0.240 17 7675181 missense variant T/A;G snv 9
rs1057519911
MAPK1
0.776 0.160 22 21772875 missense variant C/T snv 10
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 10
rs1057519926
PIK3CA
0.776 0.200 3 179210293 missense variant A/T snv 10
rs867262025
PIK3CA
0.790 0.360 3 179221146 missense variant G/A snv 10
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs1057519884
CREBBP
0.752 0.240 16 3738616 missense variant C/A;T snv 11
rs1057519886
CTNNB1
0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs121913469
ERBB2
0.763 0.240 17 39723966 missense variant TT/CC mnv 11
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