Disease: Primary malignant neoplasm
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs11263763
HNF1B
0.882 0.200 17 37743574 intron variant A/G snv 0.43 6
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1887922
IDE
0.851 0.240 10 92464408 intron variant C/T snv 0.85 6
rs1898830
TLR2
0.807 0.280 4 153687301 intron variant A/G snv 0.30 10
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs2149632
IDE
1.000 0.080 10 92472490 intron variant T/C snv 0.28 3
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs290481
TCF7L2
0.827 0.200 10 113164066 intron variant C/T snv 0.20 9
rs3745367
RETN
0.827 0.200 19 7669625 intron variant G/A snv 0.39 8
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs4704397
PDE8B
0.807 0.200 5 77222617 intron variant G/A snv 0.54 13
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs4923461
BDNF-AS ; LINC00678
0.925 0.120 11 27635363 intron variant A/C;G snv 5
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41 12
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93