Disease: Primary malignant neoplasm
Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10109984
PRKDC
0.925 0.080 8 47891114 intron variant T/C snv 0.54 4
rs11552449
AP4B1 ; DCLRE1B
0.925 0.080 1 113905767 missense variant C/G;T snv 0.22 0.15 4
rs11780156
PVT1
0.925 0.080 8 128182395 intron variant C/T snv 0.13 4
rs12945597
TOP3A
0.925 0.080 17 18271367 downstream gene variant G/A snv 0.31 4
rs1563634
SMCR8 ; TOP3A
0.925 0.080 17 18315490 5 prime UTR variant T/C;G snv 4
rs1598859
NFKB1
0.925 0.080 4 102585287 intron variant T/C snv 0.34 4
rs16886397
MAP3K1
0.925 0.080 5 56838449 intron variant A/G snv 5.8E-02 4
rs16953002
FTO
0.882 0.080 16 54080912 intron variant G/A snv 0.19 4
rs1805373
OGG1
0.925 0.080 3 9754824 missense variant G/A;C snv 6.6E-03; 4.1E-06 4
rs1805386
LIG4
0.925 0.080 13 108209565 synonymous variant A/G snv 0.13 0.14 4
rs200075329
ESR1
0.925 0.080 6 151808264 missense variant T/C snv 4.4E-03 4.3E-03 4
rs2145048 0.925 0.080 6 36589803 upstream gene variant C/A snv 0.24 4
rs2287499
WRAP53 ; TP53
0.925 0.080 17 7688850 missense variant C/G;T snv 0.20 4
rs2295079
MTOR
0.925 0.080 1 11262508 5 prime UTR variant C/G snv 0.54 4
rs2424908
DNMT3B
0.925 0.080 20 32772577 intron variant C/T snv 0.27 4
rs2532105
BLM
0.925 0.080 15 90812255 non coding transcript exon variant G/A snv 0.11 4
rs28897743
BRCA2
0.827 0.280 13 32346896 missense variant G/A;C;T snv 4.0E-06 4
rs3130932
TCF19 ; POU5F1
0.925 0.080 6 31166166 5 prime UTR variant C/A snv 0.65 0.69 4
rs3136685
CCR7
0.925 0.080 17 40563547 intron variant C/T snv 0.26 4
rs35749351
CAP1
0.925 0.080 1 40069762 missense variant G/A snv 5.7E-05 4.2E-05 4
rs3730477
DPCD ; POLL
0.925 0.080 10 101580299 missense variant G/A snv 0.17 0.16 4
rs3735615
MACC1 ; LOC101927668 ; MACC1-AS1
0.925 0.080 7 20141094 missense variant C/A;G snv 0.61 4
rs3864659
AGO2
0.925 0.080 8 140545763 intron variant A/C snv 0.16 4
rs401549
BLM
0.925 0.080 15 90813274 intron variant T/C snv 0.31 4
rs417309
DGCR8
0.925 0.080 22 20111021 3 prime UTR variant G/A snv 6.1E-02 4