Disease: Carcinoma of bladder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7439366
UGT2B7
0.752 0.320 4 69098620 missense variant T/C snv 0.56 0.57 16
rs2505568 0.851 0.160 10 36522408 non coding transcript exon variant T/A snv 0.56 4
rs7431
PPP3CC
0.882 0.120 8 22540949 3 prime UTR variant G/A snv 0.56 3
rs1014971 0.882 0.120 22 38936618 regulatory region variant C/T snv 0.55 3
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs709816
NBN
0.752 0.320 8 89955483 synonymous variant A/G snv 0.47 0.51 10
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs7212142
RPTOR
0.827 0.200 17 80650141 intron variant G/A snv 0.50 5
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs28360071
XRCC4
0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs2854744
IGFBP3
0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
rs3834129
CASP8
0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs11249206
RUNX3 ; LOC105376878
0.851 0.160 1 24951491 intron variant C/T snv 0.48 4
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs370681
AXIN1
0.807 0.200 16 342461 intron variant C/T snv 0.48 6
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs2976392
JRK ; PSCA
0.724 0.240 8 142681514 3 prime UTR variant G/A snv 0.46 0.45 15
rs12529
AKR1C3
0.776 0.280 10 5094459 missense variant C/G snv 0.50 0.45 10
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs2070584
TIMP1 ; MIR4769 ; SYN1
0.790 0.200 X 47587120 intron variant T/G snv 0.44 8
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42 9
rs7747724
CDKAL1
0.925 0.120 6 20751084 intron variant T/C snv 0.41 2