Disease: Prostate carcinoma
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
rs1012477
PER3
0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10505474
CASC8 ; PCAT1 ; POU5F1B
0.925 0.080 8 127405259 intron variant T/C snv 0.47 3
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
rs16901966
CASC19 ; PCAT1
0.925 0.080 8 127098007 intron variant A/G snv 0.13 3
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1859962
CASC17
0.882 0.160 17 71112612 intron variant G/T snv 0.56 4
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs266849
LOC105372441
0.925 0.080 19 50845834 intron variant G/A snv 0.82 4
rs2707765
APC
0.925 0.080 5 112786835 intron variant G/A;C;T snv 3
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs3774262
ADIPOQ ; ADIPOQ-AS1
0.851 0.200 3 186854025 intron variant G/A snv 0.10 5
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78 24