Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 15
rs121913272
PIK3CA
0.752 0.400 3 179210192 missense variant T/C;G snv 13
rs121913470
ERBB2
0.776 0.200 17 39723967 missense variant T/C;G snv 13
rs1057519999
TP53
0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs1057519941
PIK3CA
0.776 0.240 3 179203761 missense variant T/C;G snv 10
rs754688962
SF3B1
0.851 0.200 2 197402637 missense variant T/C;G snv 5
rs397508940
BRCA1
1.000 17 43104958 splice acceptor variant T/C;G snv 2
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs1302103336
CHEK1
0.776 0.120 11 125637491 missense variant T/C snv 8.1E-06 12
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519937
PIK3CA
0.776 0.200 3 179234285 missense variant T/C snv 11
rs80357382
BRCA1
0.763 0.240 17 43106457 missense variant T/C snv 4.0E-06 11
rs753535070
MUC1
0.851 0.120 1 155187350 missense variant T/C snv 8.0E-06 5
rs80357287
NBR2 ; BRCA1
0.882 0.200 17 43124096 start lost T/C snv 5
rs1057519857
ERBB2 ; MIR4728
0.882 0.080 17 39724772 missense variant T/C snv 4
rs13283662
UHRF2
0.925 0.080 9 6428530 intron variant T/C snv 4
rs1675126
INCENP
0.925 0.080 11 62138902 synonymous variant T/C snv 0.84 0.88 3
rs777081311
ERBB2
0.925 0.080 17 39710347 missense variant T/C snv 4.0E-06 3
rs7984952
USPL1
13 30657669 missense variant T/C snv 0.41 0.51 2
rs1057519714
ESR1
6 152094402 missense variant T/C snv 1
rs121913284
PIK3CA
0.776 0.160 3 179203765 missense variant T/A;G snv 11
rs786203071
TP53
0.776 0.240 17 7675181 missense variant T/A;G snv 9
rs1057520010
XPO1
0.882 0.200 2 61492336 missense variant T/A;G snv 5
rs80357303
BRCA1
0.925 0.200 17 43071113 stop gained T/A;G snv 4.0E-06 4
rs397507649
BRCA2
1.000 13 32337345 stop gained T/A;G snv 2