Disease: Prostate carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1571801
DAB2IP
0.827 0.120 9 121665094 intron variant G/T snv 0.21 6
rs2071203
SEMA3B
0.827 0.120 3 50274469 missense variant C/T snv 0.12 9.9E-02 6
rs212091
ABCC1
0.827 0.120 16 16142793 3 prime UTR variant T/A;C snv 5
rs2229388
MSR1
0.807 0.120 8 16155139 missense variant G/A;C snv 4.0E-06; 0.11 7
rs2239680
BIRC5
0.827 0.120 17 78223702 3 prime UTR variant T/C snv 0.27 0.24 5
rs2645429
FDFT1 ; LOC105379243
0.790 0.120 8 11802542 non coding transcript exon variant A/G;T snv 7
rs3750861
KLF6
0.827 0.120 10 3782241 intron variant C/T snv 8.2E-02 6.6E-02 5
rs9915936
AXIN2
0.827 0.120 17 65537671 synonymous variant T/C snv 0.90 0.90 5
rs1204382931
CYP1B1 ; CYP1B1-AS1
0.790 0.160 2 38075270 missense variant A/C snv 4.3E-06 10
rs7726159
TERT
0.790 0.160 5 1282204 intron variant C/A snv 0.29 10
rs2228526
ERCC6
0.752 0.200 10 49470671 missense variant T/C snv 0.22 0.19 13
rs760025060
CYP1B1 ; CYP1B1-AS1
0.776 0.200 2 38074936 missense variant C/T snv 10
rs17021918
PDLIM5
0.776 0.240 4 94641726 intron variant C/T snv 0.30 8
rs28360071
XRCC4
0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs8102476
SPINT2
0.776 0.240 19 38244973 intron variant C/T snv 0.40 8
rs9350
EXO1
0.742 0.240 1 241885372 missense variant C/T snv 0.21 0.19 16
rs10012
CYP1B1 ; CYP1B1-AS1
0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs1047840
EXO1
0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs28360317
XRCC4
0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs6869366
XRCC4 ; TMEM167A
0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs1047768
ERCC5 ; BIVM-ERCC5
0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs145204276
ZBTB37 ; SNORD74 ; SNORD75 ; GAS5 ; SNORD77 ; SNORA103 ; SNORD76
0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs213950
CFTR-AS1 ; CFTR
0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16