Disease: ovarian neoplasm
Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 48
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 22
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 14
rs587776650
NBN
0.790 0.280 8 89971214 frameshift variant GTTTT/- delins 2.0E-04 11
rs28897672
BRCA1
0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 10
rs137852986
BRIP1
0.732 0.440 17 61716051 stop gained G/A snv 1.7E-04 1.5E-04 9
rs80356898
BRCA1
0.752 0.200 17 43093844 stop gained G/A;C snv 2.8E-05; 4.0E-06 9
rs80187739
BRCA1
0.851 0.200 17 43067608 missense variant C/A;G;T snv 1.2E-05 5
rs8170
BABAM1 ; USHBP1
0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 5
rs185229225
BOD1L1
0.851 0.120 4 13607505 intron variant T/C snv 4
rs2363956
ANKLE1
0.776 0.160 19 17283315 missense variant T/G snv 0.48 0.50 4
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 4
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 3
rs113954997
RRAS2
0.882 0.280 11 14294844 missense variant T/A;C snv 3
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 3
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 3
rs2072590
HAGLR ; HAGLROS
0.851 0.120 2 176177905 non coding transcript exon variant A/C;T snv 3
rs28933370
MIR4728 ; ERBB2
0.882 0.120 17 39725125 missense variant A/G snv 7.0E-06 3
rs757210
HNF1B
0.807 0.160 17 37736525 intron variant C/G;T snv 3
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 3
rs9303542
SKAP1
0.882 0.120 17 48334138 intron variant A/G snv 0.34 3
rs137852691
OPCML
0.925 0.120 11 132657203 missense variant G/A;C snv 8.0E-06 2
rs2665390
LOC107986148 ; TIPARP
0.776 0.160 3 156679960 intron variant C/T snv 0.92 2
rs34289250
BRIP1
0.925 0.120 17 61803285 intron variant T/C snv 7.8E-03 2