Disease: Malignant Neoplasms
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12733285
ADIPOR1
0.776 0.120 1 202952912 intron variant C/T snv 0.26 12
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 18
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs1342387
ADIPOR1
0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs2270916
CASR
0.851 0.120 3 122282252 intron variant T/C snv 0.13 0.11 6
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2585428
CYP24A1
0.763 0.200 20 54170358 intron variant C/T snv 0.46 11
rs2854744
IGFBP3
0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
rs4464148
SMAD7
0.827 0.120 18 48932662 intron variant T/C snv 0.25 7
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs4809960
CYP24A1
0.807 0.240 20 54169534 intron variant T/C snv 0.20 8
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs6022999
CYP24A1
0.790 0.160 20 54171474 intron variant A/G snv 0.36 9
rs60745952
LOC107986195 ; LOC105377481
0.925 0.080 4 148827842 intron variant T/C snv 0.13 6
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9929218
CDH1
0.732 0.160 16 68787043 intron variant G/A snv 0.28 16
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs975263
MACC1
0.827 0.120 7 20158817 stop gained G/A;T snv 0.34 7