Disease: Carcinoma, Ovarian Epithelial
Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2708861
HUS1
0.851 0.120 7 47977120 intron variant T/G snv 0.46 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
rs1467465
THEMIS2
0.827 0.160 1 27884892 non coding transcript exon variant A/G snv 0.61 7
rs1469713
GATAD2A
0.827 0.160 19 19417997 intron variant A/G snv 0.44 6
rs200182588
SMC2-AS1 ; SMC2
0.827 0.160 9 104094409 5 prime UTR variant -/GC ins 7.0E-06 6
rs28997576
BARD1
0.776 0.160 2 214752454 missense variant C/G;T snv 1.5E-02 11
rs5013329
NSUN4
0.827 0.160 1 46349419 intron variant C/T snv 0.23 6
rs748876625
BRCA1
0.807 0.160 17 43104122 missense variant C/A;G snv 1.2E-05 9
rs8037137
RCCD1
0.807 0.160 15 90963407 upstream gene variant T/C snv 0.19 6
rs9375701
L3MBTL3
0.827 0.160 6 130062912 intron variant C/T snv 0.53 6
rs16949649
NME1 ; NME1-NME2
0.776 0.200 17 51152947 upstream gene variant T/C snv 0.39 12
rs267607911
MSH2
0.851 0.200 2 47403192 start lost A/C;G;T snv 5.1E-05; 1.4E-05 8
rs28897696
BRCA1
0.807 0.200 17 43063903 missense variant G/A;C;T snv 2.8E-05; 4.0E-06; 2.0E-05 7
rs3020450
ESR2
0.807 0.200 14 64301584 splice region variant C/A;T snv 10
rs7937840
INCENP
0.807 0.200 11 62126500 intron variant C/T snv 0.20 6
rs7958904
HOTAIR
0.724 0.200 12 53963768 non coding transcript exon variant C/A;G snv 15
rs1799950
BRCA1
0.752 0.240 17 43094464 missense variant T/C snv 4.7E-02 4.6E-02 13
rs2229109
ABCB1
0.807 0.240 7 87550493 missense variant C/A;T snv 2.7E-02 8
rs2302254
NME1-NME2 ; NME1
0.752 0.240 17 51153539 5 prime UTR variant C/T snv 0.22 15
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 8
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 8
rs851797
EXO1
0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 33