Disease: Carcinoma of bladder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs150799650
CYP1B1 ; CYP1B1-AS1
0.925 0.120 2 38073618 non coding transcript exon variant G/T snv 7.0E-05 2
rs1937920 0.925 0.120 10 5119763 downstream gene variant A/G snv 0.28 2
rs2836007
KCNJ6
0.925 0.120 21 37834589 intron variant C/T snv 0.21 2
rs4510656
CDKAL1
0.925 0.120 6 20766466 intron variant C/A snv 0.39 2
rs5003154
PAG1
0.925 0.120 8 81074718 intron variant T/C;G snv 2
rs6104690
LINC02871
0.925 0.120 20 11007451 intron variant G/A;T snv 2
rs7238033
SLC14A1 ; LOC105372093
0.925 0.120 18 45737001 intron variant T/C snv 0.61 2
rs7747724
CDKAL1
0.925 0.120 6 20751084 intron variant T/C snv 0.41 2
rs1014971 0.882 0.120 22 38936618 regulatory region variant C/T snv 0.55 3
rs10234749 0.882 0.120 7 152690784 regulatory region variant T/C;G snv 3
rs10775480
LOC105372093 ; SLC14A1
0.882 0.120 18 45737317 intron variant T/C snv 0.61 3
rs11077654
SLC39A11
0.882 0.120 17 73010373 intron variant A/C snv 0.69 3
rs11191438
AS3MT ; BORCS7-ASMT
0.882 0.120 10 102878107 intron variant G/A;C snv 3
rs1135612
POR
0.882 0.120 7 75980359 synonymous variant A/G;T snv 0.28 3
rs11543198
CLK3
0.882 0.120 15 74619987 missense variant G/A;T snv 0.11 3
rs11871756
SLC39A11
0.882 0.120 17 72730105 intron variant C/G snv 0.11 3
rs1189516787
CEBPA ; CEBPA-DT
0.882 0.120 19 33301681 missense variant C/G snv 7.1E-06 3
rs1203030830
EGFR
0.882 0.120 7 55155873 synonymous variant T/C snv 4.0E-06 3
rs1336331763
SULT1A1
0.882 0.120 16 28606796 missense variant G/A snv 4.0E-06 3
rs140241283
MTHFR
0.882 0.120 1 11796249 start lost A/G;T snv 4.0E-06; 4.0E-06 3
rs1428779969
PXN
0.882 0.120 12 120223776 missense variant G/A snv 7.0E-06 3
rs1484761909
GSTM1 ; GSTM2
0.882 0.120 1 109688224 missense variant A/G snv 3.0E-05 3.8E-05 3
rs17650301
POLG2 ; MILR1
0.925 0.120 17 64483156 intron variant A/C snv 0.23 3
rs17674580
SLC14A1 ; LOC105372093
0.882 0.120 18 45729946 5 prime UTR variant C/A;T snv 3
rs197414
DDX20
0.882 0.120 1 111766501 missense variant C/A;T snv 0.12; 4.0E-06 3