Disease: Bladder Neoplasm
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1109324 0.827 0.160 6 43762018 intergenic variant G/T snv 0.15 5
rs754554026
MLH1
0.827 0.160 3 37028864 missense variant G/A;C snv 2.8E-05 7.0E-06 5
rs833052 0.827 0.160 6 43755598 intergenic variant A/C snv 0.88 5
rs2978974
JRK ; PSCA
0.790 0.200 8 142670446 non coding transcript exon variant G/A snv 0.38 7
rs8679
PARP1
0.790 0.200 1 226360853 3 prime UTR variant A/G snv 0.16 7
rs1046428
GSTZ1
0.776 0.200 14 77327940 missense variant T/A;C snv 4.0E-06; 0.81 8
rs3136820
APEX1
0.776 0.200 14 20456995 missense variant T/A;C;G snv 8
rs6443624
PIK3CA
0.776 0.200 3 179179886 intron variant C/A snv 0.30 8
rs1057868
POR
0.763 0.320 7 75985688 missense variant C/T snv 0.31 0.27 9
rs11685387
XRCC5
0.776 0.240 2 216109091 splice region variant C/T snv 0.30 9
rs7975
GSTZ1
0.763 0.320 14 77326864 stop gained G/A;C;T snv 0.31 0.32 9
rs80357138
BRCA1
0.763 0.200 17 43094776 missense variant C/T snv 8.0E-06 9
rs9288518
XRCC5
0.776 0.240 2 216196997 intron variant A/G snv 0.35 9
rs2155209
MRE11
0.776 0.240 11 94417624 3 prime UTR variant T/C snv 0.27 10
rs3731239
CDKN2A
0.763 0.240 9 21974219 intron variant A/G snv 0.26 10
rs386675647
UGT2B7
0.790 0.240 4 69098619 missense variant AT/TC mnv 10
rs709816
NBN
0.752 0.320 8 89955483 synonymous variant A/G snv 0.47 0.51 10
rs10511729
LOC101929563
0.742 0.240 9 23557229 intron variant T/G snv 0.35 11
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs12683422
LINGO2
0.742 0.240 9 27969442 intron variant C/T snv 5.7E-02 11
rs25648
VEGFA
0.742 0.320 6 43771240 synonymous variant C/G;T snv 8.5E-06; 0.16 11
rs744154
ERCC4
0.763 0.280 16 13921224 intron variant G/C snv 0.23 11
rs776223836
ERCC2
0.763 0.280 19 45364045 missense variant G/A snv 11
rs1799794
XRCC3 ; KLC1
0.763 0.320 14 103712930 splice region variant T/C snv 0.22 12
rs3136817
APEX1 ; OSGEP
0.732 0.280 14 20456275 intron variant T/C snv 0.23 12