Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519988
TP53
0.776 0.240 17 7673812 missense variant A/C;G;T snv 10
rs1057519997
TP53
0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs28897672
BRCA1
0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 9
rs876659675
TP53
0.807 0.280 17 7674199 missense variant A/C;G;T snv 7
rs397509173
BRCA1
0.925 0.200 17 43104120 splice donor variant A/C;G;T snv 4
rs80357006
BRCA1
0.925 0.200 17 43092274 stop gained A/C;G;T snv 1.2E-05 4
rs1057520004
TP53
0.752 0.240 17 7674884 missense variant A/C;T snv 11
rs1057519938
PIK3CA
0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv 5
rs587781632
BRCA1
0.925 0.200 17 43106476 splice donor variant A/C;T snv 4
rs41293463
BRCA1
0.790 0.280 17 43051071 missense variant A/C;T snv 1.2E-05 3
rs2273535
AURKA
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 1
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519933
PIK3CA
0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519935
PIK3CA
0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519960
SF3B2
0.827 0.280 11 66063413 missense variant A/G snv 7
rs1057519914
MTOR
0.851 0.240 1 11157174 missense variant A/G snv 4
rs1057519727
HERC2
15 28260829 missense variant A/G snv 1
rs1057520036
FGFR4
0.925 0.080 5 177093180 missense variant A/G snv 1
rs121913288
PIK3CA
1.000 0.200 3 179234219 missense variant A/G snv 1
rs1555582520
BRCA1
17 43076486 splice donor variant A/G snv 1
rs796065354
ESR1
0.882 0.080 6 151944320 missense variant A/G snv 1
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs1057519936
PIK3CA
0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs80357086
BRCA1
0.851 0.200 17 43106480 stop gained A/G;T snv 4