Disease: Malignant neoplasm of prostate
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
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
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
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs1197734477
PTEN
0.925 0.080 10 87961012 missense variant A/G snv 4
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
rs12338
CTSB
0.807 0.200 8 11853379 missense variant G/A;C;T snv 8.0E-06; 0.38; 2.4E-05 10
rs12422149
SLCO2B1
0.827 0.120 11 75172532 missense variant G/A;T snv 0.18 7
rs1290923018
ZNRD2 ; ZNRD2-AS1 ; FAM89B
0.851 0.160 11 65570699 missense variant G/A snv 4.0E-06 5
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1353702185
MDM2
0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 9
rs137852581
AR
0.882 0.080 X 67723701 missense variant C/T snv 4
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 28
rs1450063773
KLK3
0.925 0.080 19 50858491 missense variant C/A;T snv 8.0E-06; 4.0E-06 3
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
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv 15