Disease: Malignant neoplasm of prostate
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10505474
CASC8 ; PCAT1 ; POU5F1B
0.925 0.080 8 127405259 intron variant T/C snv 0.47 3
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs1060501201
TP53
0.925 0.080 17 7674190 missense variant T/C;G snv 4
rs11902171
ITGAV
0.925 0.080 2 186678500 3 prime UTR variant G/C snv 0.22 6
rs1197734477
PTEN
0.925 0.080 10 87961012 missense variant A/G snv 4
rs12757998 0.925 0.080 1 182569343 downstream gene variant C/T snv 0.24 3
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs137852581
AR
0.882 0.080 X 67723701 missense variant C/T snv 5
rs1450063773
KLK3
0.925 0.080 19 50858491 missense variant C/A;T snv 8.0E-06; 4.0E-06 3
rs149709822
KLK3
0.882 0.080 19 50856335 missense variant G/A snv 4.0E-05 2.3E-04 4
rs16901966
CASC19 ; PCAT1
0.925 0.080 8 127098007 intron variant A/G snv 0.13 3
rs17632542
KLK3
0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 5
rs1902023
UGT2B15
0.882 0.080 4 68670366 missense variant A/C snv 0.51 0.53 4
rs266849
LOC105372441
0.925 0.080 19 50845834 intron variant G/A snv 0.82 4
rs267605077
TP53
0.925 0.080 17 7675212 missense variant A/G;T snv 3
rs2707765
APC
0.925 0.080 5 112786835 intron variant G/A;C;T snv 3
rs3747531
MSR1
0.925 0.080 8 16155139 missense variant G/A;C snv 3
rs41441651
BTNL2 ; TSBP1-AS1
0.925 0.080 6 32396111 missense variant C/T snv 2.3E-02 9.5E-03 3
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 16
rs627928
RNASEL
0.790 0.080 1 182582202 missense variant A/C snv 0.54 0.49 10
rs6470517
CASC8
0.925 0.080 8 127448159 intron variant A/G snv 0.15 3
rs822391
ADIPOQ
0.925 0.080 3 186846014 intron variant C/T snv 0.85 4
rs9600079 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 5
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs12422149
SLCO2B1
0.827 0.120 11 75172532 missense variant G/A;T snv 0.18 7