Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs9642880
CASC11
0.776 0.240 8 127705823 intron variant G/A;T snv 9
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 24
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 16
rs867262025
PIK3CA
0.790 0.360 3 179221146 missense variant G/A snv 10
rs866987936
FBXW7
0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs80359601
BRCA2
0.807 0.360 13 32340890 frameshift variant -/A;NNNNNNNN ins 4.1E-06 8
rs798766
TACC3
0.851 0.120 4 1732512 intron variant T/C snv 0.76 6
rs786203071
TP53
0.776 0.240 17 7675181 missense variant T/A;G snv 9
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 21
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 24
rs786201419
TP53
0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 20
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs775623976
SF3B1
0.851 0.240 2 197402760 missense variant G/A;C snv 4.0E-06 4
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25
rs759610249
FBXW7
0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs750802459
CASP3
1.000 0.120 4 184635342 frameshift variant TCAGGATAATCCATTTTATAACTGTTGTCCAGGGATATTCCAGAGTC/- delins 5.6E-05 2
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21