Disease: Malignant neoplasm of prostate
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11536891
TLR4
0.851 0.120 9 117717059 3 prime UTR variant T/C snv 0.16 4
rs540635787
CHEK2
0.851 0.200 22 28694073 missense variant G/A;C;T snv 1.7E-05 4
rs758081262
ATM
0.851 0.360 11 108267258 stop gained C/T snv 1.2E-05 4
rs11574143
VDR
0.827 0.200 12 47841134 downstream gene variant C/T snv 0.11 5
rs117251022
ARL11
0.827 0.120 13 49630641 missense variant G/A;C;T snv 8.8E-05; 1.9E-03 5
rs406193 0.882 0.120 20 32811837 downstream gene variant T/C snv 0.91 5
rs55829688
SNORD77 ; SNORA103 ; ZBTB37 ; SNORD76 ; SNORD74 ; SNORD75 ; GAS5
0.827 0.200 1 173868168 5 prime UTR variant T/C;G snv 5
rs6147150
ERBB4
0.827 0.160 2 211380365 3 prime UTR variant -/AAAATAGGATTG delins 5
rs7000448
CASC8
0.827 0.160 8 127428925 intron variant C/T snv 0.45 5
rs7008482
NSMCE2
0.882 0.120 8 125255388 intron variant T/G snv 0.48 5
rs768362387
ATM
0.851 0.360 11 108253846 stop gained C/A snv 5
rs8752
HPGD
0.827 0.160 4 174491326 3 prime UTR variant C/T snv 0.49 5
rs7579
CCDC152 ; SELENOP
0.807 0.200 5 42800706 3 prime UTR variant C/T snv 0.31 0.26 6
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs14133
HSPB2-C11orf52 ; CRYAB ; HSPB2
0.807 0.200 11 111911973 5 prime UTR variant G/C snv 0.27 7
rs4775936
MIR4713HG ; CYP19A1
0.790 0.200 15 51243825 intron variant C/T snv 0.36 7
rs13252298
PCAT2 ; PCAT1 ; PRNCR1 ; CASC19
0.827 0.160 8 127082911 non coding transcript exon variant A/G snv 0.24 8
rs748500299
PTGS2
0.790 0.200 1 186675960 missense variant T/A;C snv 4.0E-06; 4.0E-06 8
rs7837328
CASC8 ; PCAT1 ; POU5F1B
0.882 0.120 8 127410882 intron variant A/G snv 0.52 8
rs1456315
PRNCR1 ; PCAT1 ; CASC19
0.790 0.200 8 127091692 non coding transcript exon variant T/A;C snv 9
rs1982151
RMI1
0.807 0.120 9 84002350 missense variant A/G;T snv 0.73 9
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 9
rs6022999
CYP24A1
0.790 0.160 20 54171474 intron variant A/G snv 0.36 9
rs760025060
CYP1B1 ; CYP1B1-AS1
0.776 0.200 2 38074936 missense variant C/T snv 10
rs822395
ADIPOQ
0.776 0.240 3 186849018 intron variant C/A;G snv 10