Disease: ovarian neoplasm
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 11
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 9
rs2699887
PIK3CA ; LOC101928739
0.763 0.280 3 179148620 intron variant C/T snv 0.18 11
rs2708861
HUS1
0.851 0.120 7 47977120 intron variant T/G snv 0.46 6
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs3020450
ESR2
0.807 0.200 14 64301584 splice region variant C/A;T snv 10
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4143815
CD274
0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23 20
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs5013329
NSUN4
0.827 0.160 1 46349419 intron variant C/T snv 0.23 6
rs540432391
CGB5
0.882 0.120 19 49043993 5 prime UTR variant G/A;C snv 5
rs587782529
TP53
0.851 0.200 17 7670700 missense variant G/A;C snv 8
rs61764370
KRAS
0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs7246045
CGB5
0.882 0.120 19 49042825 upstream gene variant T/G snv 2.9E-02 5
rs7937840
INCENP
0.807 0.200 11 62126500 intron variant C/T snv 0.20 7
rs80356913
BRCA1
0.851 0.200 17 43106456 missense variant C/A;G;T snv 7
rs8037137
RCCD1
0.807 0.160 15 90963407 upstream gene variant T/C snv 0.19 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
rs876659384
TP53
0.851 0.240 17 7673552 stop gained C/A snv 7
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32