Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519928
PIK3CA
0.807 0.200 3 179221147 missense variant A/C snv 8
rs1057519915
MTOR
0.851 0.160 1 11109318 missense variant A/C snv 5
rs1057519959
SF3B2
0.882 0.200 11 66063028 missense variant A/C snv 4
rs11895168
ERBB4
0.925 0.080 2 211377467 3 prime UTR variant A/C snv 0.68 4
rs121913282
PIK3CA
0.882 0.040 3 179221072 missense variant A/C snv 4
rs2787486
STXBP4
0.925 0.080 17 55132413 intron variant A/C snv 0.33 3
rs146312682
LIMD1
3 45595642 missense variant A/C snv 8.6E-04 7.7E-04 1
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057519986
TP53
0.776 0.240 17 7673811 missense variant A/C;G snv 10
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 9
rs80357243
BRCA1
17 43063885 missense variant A/C;G snv 2
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs28897672
BRCA1
0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 16
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 16