Disease: Malignant Neoplasms
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 7
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs132793 0.851 0.160 22 41667677 downstream gene variant A/C;G;T snv 7
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs2069514 0.807 0.160 15 74745879 upstream gene variant G/A snv 0.13 9
rs2145048 0.925 0.080 6 36589803 upstream gene variant C/A snv 0.24 4
rs2410373 0.851 0.120 8 16066997 intergenic variant A/C snv 0.34 6
rs28714259 0.882 0.120 15 23463380 intergenic variant G/A snv 0.19 5
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs9325782 0.851 0.120 8 16232964 intron variant C/T snv 0.87 6
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
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
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs1693482
ADH1C ; ADH1B
0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs7539542
ADIPOR1
0.807 0.200 1 202940846 3 prime UTR variant G/C snv 0.58 9
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65