Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs786201419
TP53
0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs180177040
BRAF
0.790 0.360 7 140754187 missense variant T/C;G snv 9
rs1057519947
PPP2R1A
0.790 0.160 19 52212730 missense variant G/A snv 9
rs786203071
TP53
0.776 0.240 17 7675181 missense variant T/A;G snv 9
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519877
B2M ; PATL2
0.763 0.280 15 44711549 start lost G/A snv 10
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 10
rs1057519879
PATL2 ; B2M
0.763 0.280 15 44711548 start lost T/C;G snv 10
rs1057519986
TP53
0.776 0.240 17 7673811 missense variant A/C;G snv 10
rs1057519987
TP53
0.776 0.280 17 7673810 missense variant A/C snv 10
rs1057519988
TP53
0.776 0.240 17 7673812 missense variant A/C;G;T snv 10
rs587782177
TP53
0.763 0.200 17 7674887 missense variant C/A;G;T snv 11
rs1057519896
FBXW7
0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs1057519999
TP53
0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs1057520004
TP53
0.752 0.240 17 7674884 missense variant A/C;T snv 12
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 14
rs867384286
FBXW7
0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 14
rs1057520005
TP53
0.742 0.360 17 7673800 missense variant C/A;G snv 14
rs1057520006
TP53
0.752 0.240 17 7673799 missense variant A/C;G;T snv 14
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv 15
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 15