Disease: Neoplasms
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 11
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs4415084 0.827 0.080 5 44662413 upstream gene variant C/T snv 0.49 6
rs554219 0.925 0.080 11 69516874 regulatory region variant C/A;G;T snv 3
rs614367 0.882 0.080 11 69513996 intergenic variant C/T snv 0.14 4
rs62355902 1.000 0.080 5 56757896 intergenic variant A/T snv 0.15 2
rs7716600 0.925 0.080 5 44874903 regulatory region variant A/C;T snv 4
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs765189442
ABCB11
0.925 0.080 2 168995422 missense variant T/C snv 8.1E-06 4
rs17822931
ABCC11
0.827 0.080 16 48224287 missense variant C/G;T snv 4.0E-06; 0.22 0.13 7
rs2273697
ABCC2
0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 11
rs717620
ABCC2
0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs184003
AGER
0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36