Disease: Prostate carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17115149
CYP17A1
0.882 0.160 10 102837961 upstream gene variant G/A;T snv 4
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 9
rs4410790
LOC101927609 ; AHR
0.882 0.160 7 17244953 intron variant T/C snv 0.54 9
rs750392184
PIK3CD
0.882 0.160 1 9724850 missense variant G/A snv 4.0E-06 3
rs11263763
HNF1B
0.882 0.200 17 37743574 intron variant A/G snv 0.43 6
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50 7
rs11536858 0.851 0.240 9 117701869 upstream gene variant G/A;T snv 4
rs12500426
PDLIM5
0.851 0.240 4 94593458 intron variant A/C snv 0.54 5
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 12
rs822395
ADIPOQ
0.776 0.240 3 186849018 intron variant C/A;G snv 10
rs849136
JAZF1
0.851 0.240 7 28135338 intron variant A/G snv 0.74 4
rs849140
JAZF1
0.851 0.240 7 28144083 intron variant T/C snv 0.58 7
rs849141
JAZF1
0.851 0.240 7 28145472 intron variant A/G snv 0.78 6
rs1799941
SHBG
0.763 0.280 17 7630105 5 prime UTR variant G/A snv 0.18 11
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41 12
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 7
rs2853669
TERT
0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 12
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs2248359
CYP24A1
0.790 0.400 20 54174979 upstream gene variant C/T snv 0.47 8
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs6259
SHBG
0.658 0.400 17 7633209 missense variant G/A snv 8.9E-02 8.1E-02 27
rs822396
ADIPOQ
0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 19