Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs1057520006
TP53
0.752 0.240 17 7673799 missense variant A/C;G;T snv 14
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
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
rs876659675
TP53
0.807 0.280 17 7674199 missense variant A/C;G;T snv 8
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
rs2273535
AURKA
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs6505162
NSRP1 ; MIR3184 ; MIR423
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs1057520004
TP53
0.752 0.240 17 7674884 missense variant A/C;T snv 12
rs1057519938
PIK3CA
0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs41293463
BRCA1
0.790 0.280 17 43051071 missense variant A/C;T snv 1.2E-05 9
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv 7
rs587781632
BRCA1
0.925 0.200 17 43106476 splice donor variant A/C;T snv 4
rs7716600 0.925 0.080 5 44874903 regulatory region variant A/C;T snv 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
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
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 11
rs796065354
ESR1
0.882 0.080 6 151944320 missense variant A/G snv 9