Disease: ovarian neoplasm
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 4
rs10098821
LINC00824
0.882 0.120 8 128546982 intron variant C/T snv 7.6E-02 3
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs11084033
LOC105372441
0.882 0.120 19 50850699 intron variant C/A;T snv 4
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 9
rs11655505
NBR2 ; BRCA1
0.776 0.160 17 43126360 intron variant G/A snv 0.31 8
rs11683487
NMI
0.882 0.120 2 151286035 intron variant G/T snv 0.36 3
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 4
rs11954856
APC
0.732 0.200 5 112751630 intron variant T/G snv 0.54 12
rs12373237
LAMA3
0.851 0.200 18 23845972 intron variant G/A snv 0.47 5
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 7
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs13063604
RUVBL1
0.882 0.120 3 128085887 intron variant G/A snv 0.23 3
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs1469713
GATAD2A
0.827 0.160 19 19417997 intron variant A/G snv 0.44 7
rs1516982
LINC00824
0.882 0.120 8 128521400 intron variant A/G snv 0.16 3
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs185229225
BOD1L1
0.851 0.120 4 13607505 intron variant T/C snv 4
rs186724
AHCYL1
0.882 0.120 1 110018293 intron variant C/G;T snv 3
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs1989839
ZMYND10 ; RASSF1
0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20 8