Disease: Prostate carcinoma
Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs10483813
RAD51B
0.851 0.120 14 68564567 intron variant T/A;C snv 4
rs11133373
SRD5A3
0.851 0.120 4 55349464 intron variant C/G;T snv 4
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 33
rs1194022307
FOLH1
0.851 0.120 11 49146838 missense variant G/A snv 4.0E-06 4
rs1204382931
CYP1B1 ; CYP1B1-AS1
0.790 0.160 2 38075270 missense variant A/C snv 4.3E-06 10
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 83
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 26
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs13254738
PRNCR1 ; CASC19 ; PCAT1
0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv 8
rs1353702185
MDM2
0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1394960893
GSTP1
0.807 0.240 11 67586553 synonymous variant C/T snv 6
rs1445081098
COMT ; MIR4761
0.724 0.480 22 19963746 missense variant G/C snv 4.0E-06 17
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 28
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
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
rs16917496
KMT5A
0.689 0.360 12 123409283 3 prime UTR variant C/G;T snv 21
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72