Disease: Prostate carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
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
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799941
SHBG
0.763 0.280 17 7630105 5 prime UTR variant G/A snv 0.18 11
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs2023305
CCR6
0.851 0.280 6 167111410 intron variant C/T snv 0.38 4
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2745557
PACERR ; PTGS2
0.807 0.200 1 186680089 intron variant A/G snv 0.83 6
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs7613548
LZTFL1 ; CCR9
0.882 0.160 3 45885077 intron variant G/A;C snv 3
rs7799039
LOC105375494
0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs822396
ADIPOQ
0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98