Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs878853297
BRCA2
0.925 0.200 13 32319166 frameshift variant AA/-;A;AAA delins 4
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs876660254
TP53
0.882 0.040 17 7674963 missense variant G/T snv 4
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 16
rs876659675
TP53
0.807 0.280 17 7674199 missense variant A/C;G;T snv 8
rs876659036
PALB2
1.000 0.080 16 23622997 stop gained C/A;G snv 8.0E-06; 8.0E-06 3
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 24
rs867384286
FBXW7
0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
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
rs864622401
BRCA2
0.882 0.200 13 32339092 frameshift variant -/TG delins 4
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
rs8133052
CBR3 ; CBR3-AS1
0.925 0.120 21 36135203 missense variant G/A;C snv 0.44 6
rs81002796
BRCA2
0.925 0.200 13 32316528 splice donor variant G/A;C;T snv 4
rs80359759
BRCA2
0.925 0.200 13 32394832 frameshift variant G/- delins 4
rs80359706
BRCA2
1.000 13 32363522 frameshift variant -/T delins 3
rs80359603
BRCA2
1.000 13 32340907 frameshift variant G/- delins 2
rs80359584
BRCA2
0.807 0.280 13 32340757 frameshift variant CTTAA/- delins 4.2E-06 1.4E-05 8
rs80359550
BRCA2
0.807 0.280 13 32340301 frameshift variant T/- del 1.8E-04 8
rs80359351
BRCA2
0.851 0.200 13 32337161 frameshift variant ACAA/- delins 2.1E-05 6