Disease: Primary malignant neoplasm
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1063538
ADIPOQ ; ADIPOQ-AS1
1.000 0.080 3 186856394 3 prime UTR variant T/C snv 0.55 4
rs2149632
IDE
1.000 0.080 10 92472490 intron variant T/C snv 0.28 3
rs1892534
LEPR
0.925 0.120 1 65640261 3 prime UTR variant C/T snv 0.44 7
rs4923461
BDNF-AS ; LINC00678
0.925 0.120 11 27635363 intron variant A/C;G snv 5
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 8
rs11263763
HNF1B
0.882 0.200 17 37743574 intron variant A/G snv 0.43 6
rs290481
TCF7L2
0.827 0.200 10 113164066 intron variant C/T snv 0.20 9
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 9
rs3745367
RETN
0.827 0.200 19 7669625 intron variant G/A snv 0.39 8
rs4704397
PDE8B
0.807 0.200 5 77222617 intron variant G/A snv 0.54 13
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs869109213
NOS3
0.790 0.200 7 150997269 intron variant GGGGGTGAGGAAGTCTAGACCTGCTGCG/A delins 10
rs1044250
ANGPTL4
0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 12
rs1887922
IDE
0.851 0.240 10 92464408 intron variant C/T snv 0.85 6
rs7158663
MEG3
0.827 0.240 14 100853087 non coding transcript exon variant A/G snv 0.42 9
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs822395
ADIPOQ
0.776 0.240 3 186849018 intron variant C/A;G snv 10
rs1799941
SHBG
0.763 0.280 17 7630105 5 prime UTR variant G/A snv 0.18 11
rs1898830
TLR2
0.807 0.280 4 153687301 intron variant A/G snv 0.30 10
rs2108622
CYP4F2
0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 20
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24