Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80359176
BRCA2
1.000 0.120 13 32380076 missense variant C/T snv 3.6E-05 7.0E-06 1
rs4987046
BRCA2
0.925 0.160 13 32319134 missense variant A/G snv 1.6E-03 1.6E-03 4
rs6886
CAPG
0.925 0.160 2 85394936 missense variant T/A;C snv 0.58 4
rs2153271
BNC2
0.925 0.160 9 16864523 intron variant C/T snv 0.43 3
rs80356993
BRCA1
0.925 0.120 17 43063937 missense variant A/G;T snv 3
rs869312756
ATM
0.925 0.320 11 108307985 splice donor variant G/A;T snv 3
rs869312774
PALB2
0.925 0.160 16 23614019 frameshift variant T/- delins 3
rs137852691
OPCML
0.925 0.120 11 132657203 missense variant G/A;C snv 8.0E-06 2
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
rs34289250
BRIP1
0.925 0.120 17 61803285 intron variant T/C snv 7.8E-03 2
rs41293521
BRCA2
0.925 0.160 13 32394724 missense variant T/C snv 2.9E-04 2.5E-04 2
rs771386507
HLA-B ; MIR6891
0.882 0.120 6 31355479 missense variant C/T snv 4.0E-06 6
rs540432391
CGB5
0.882 0.120 19 49043993 5 prime UTR variant G/A;C snv 5
rs7246045
CGB5
0.882 0.120 19 49042825 upstream gene variant T/G snv 2.9E-02 5
rs11084033
LOC105372441
0.882 0.120 19 50850699 intron variant C/A;T snv 4
rs121913322
STK11
0.882 0.120 19 1221320 missense variant C/A;G;T snv 2.9E-05; 1.2E-04 4
rs1444192401
KRT7
0.882 0.120 12 52235347 missense variant G/A snv 4
rs2287498
WRAP53 ; TP53
0.882 0.120 17 7689242 synonymous variant C/T snv 0.13 0.14 4
rs495139
ENOSF1
0.882 0.120 18 676008 intron variant G/C snv 0.63 4
rs4988344
BRIP1
0.882 0.120 17 61847251 intron variant G/C snv 0.20 0.15 4
rs6785617 0.882 0.120 3 172501054 downstream gene variant A/T snv 3.7E-02 4
rs74315464
ARSA
0.882 0.120 22 50627048 missense variant G/A;C snv 4
rs80357233
BRCA1
0.882 0.200 17 43093393 stop gained G/C;T snv 4.0E-06 4
rs10098821
LINC00824
0.882 0.120 8 128546982 intron variant C/T snv 7.6E-02 3