Disease: Neoplasm Metastasis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs35301225
MIR34A ; MIR34AHG
0.882 0.080 1 9151743 mature miRNA variant C/A;T snv 5
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs992157
TMBIM1 ; PNKD
0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 10
rs1800734
EPM2AIP1 ; MLH1
0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs752021744
PIK3CB
0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs3775292
TLR3
0.851 0.080 4 186081871 non coding transcript exon variant C/G snv 0.82 5
rs60745952
LOC107986195 ; LOC105377481
0.925 0.080 4 148827842 intron variant T/C snv 0.13 6
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs629849
IGF2R
0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 9
rs77191406
TNFAIP3
0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv 16
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs28929495
EGFR
0.807 0.120 7 55174014 missense variant G/A;C;T snv 9
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14