Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs273900729
BRCA1
0.925 0.160 17 43082529 missense variant A/G snv 2
rs28897701
BRCA2
0.925 0.160 13 32319232 missense variant G/C snv 2.6E-04 3.1E-04 2
rs41293521
BRCA2
0.925 0.160 13 32394724 missense variant T/C snv 2.9E-04 2.5E-04 2
rs1064795649
BRIP1
1.000 0.120 17 61799205 frameshift variant CT/- delins 2
rs34289250
BRIP1
0.925 0.120 17 61803285 intron variant T/C snv 7.8E-03 2
rs137852691
OPCML
0.925 0.120 11 132657203 missense variant G/A;C snv 8.0E-06 2
rs4954956 0.882 0.120 2 138787007 regulatory region variant C/T snv 0.25 3
rs7365052 0.882 0.120 1 236786561 intergenic variant T/C snv 3
rs35068177
ABCB1
0.882 0.120 7 87550213 synonymous variant T/C snv 2.2E-04 3.1E-04 3
rs186724
AHCYL1
0.882 0.120 1 110018293 intron variant C/G;T snv 3
rs351771
APC
0.882 0.120 5 112828864 synonymous variant G/A snv 0.65 0.59 3
rs751039340
ARSA
0.882 0.120 22 50625459 missense variant C/A snv 4.2E-06 3
rs869312756
ATM
0.925 0.320 11 108307985 splice donor variant G/A;T snv 3
rs2153271
BNC2
0.925 0.160 9 16864523 intron variant C/T snv 0.43 3
rs567534295
BRCA1
0.882 0.120 17 43048090 intron variant C/T snv 2.8E-05 3
rs80356993
BRCA1
0.925 0.120 17 43063937 missense variant A/G;T snv 3
rs80357828
BRCA1
0.882 0.200 17 43092155 frameshift variant GA/- delins 3
rs879255288
BRCA1
0.882 0.120 17 43094789 missense variant T/C;G snv 4.0E-06 3
rs55854959
BRCA2
0.882 0.120 13 32330979 missense variant G/A snv 2.4E-05 1.4E-04 3
rs80359078
BRCA2
0.882 0.160 13 32370430 missense variant G/A snv 3.2E-05 2.1E-05 3
rs876658943
BRCA2
0.882 0.120 13 32332593 missense variant A/G snv 4.0E-06 3
rs2191249
BRIP1
0.882 0.120 17 61758503 intron variant T/G snv 0.79 3
rs121964872
CDH1
0.882 0.120 16 68833362 missense variant A/G snv 4.4E-05 1.1E-04 3
rs34529039
CEBPA ; CEBPA-DT
0.882 0.120 19 33301725 synonymous variant C/A snv 0.19 0.16 3
rs7260002
CGB5
0.882 0.120 19 49042615 non coding transcript exon variant A/C;G snv 0.46 3