Disease: Neoplasms
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11977670
LOC107986854
1.000 0.080 7 140242504 downstream gene variant G/A snv 0.39 2
rs62355902 1.000 0.080 5 56757896 intergenic variant A/T snv 0.15 2
rs1011329790
GGCT
0.925 0.080 7 30504681 missense variant G/A snv 3
rs1057090
MCPH1 ; MCPH1-AS1
0.925 0.080 8 6621521 missense variant C/A;G;T snv 4.0E-06; 0.43 3
rs1060502346
BRCA1
0.925 0.080 17 43106513 missense variant A/G snv 3
rs11141901
DAPK1
0.925 0.080 9 87575750 intron variant A/G snv 0.28 3
rs114729114
BRAF
0.925 0.080 7 140910797 intron variant C/T snv 1.1E-02 3
rs1159579789
TP53
0.925 0.080 17 7673578 missense variant T/C snv 4.0E-06 3
rs1207112399
ESR1
0.925 0.080 6 151842614 missense variant G/A snv 4.0E-06 7.0E-06 3
rs120963
NDUFAB1
0.925 0.080 16 23596749 upstream gene variant A/G snv 0.28 3
rs12922061
CASC16
0.925 0.080 16 52601088 intron variant C/T snv 0.19 3
rs141047069
PALB2
0.925 0.080 16 23638074 missense variant A/G snv 3
rs1430450850
COL11A2
0.925 0.080 6 33165971 missense variant G/A snv 3
rs1458567397
RGSL1
0.925 0.080 1 182530861 missense variant C/T snv 1.9E-05 3
rs148972953
LAMTOR3
0.925 0.080 4 99881589 3 prime UTR variant A/G snv 8.8E-03 3
rs15869
BRCA2
0.925 0.080 13 32398875 3 prime UTR variant A/C snv 0.15 3
rs17227210
RUNX1
0.925 0.080 21 35051694 intron variant C/T snv 0.11 3
rs17468277
FLACC1
0.925 0.080 2 201289477 synonymous variant C/A;T snv 4.0E-06; 9.0E-02 3
rs181088346
TSC2
0.925 0.080 16 2069770 intron variant G/A snv 2.3E-02 3
rs1964676
LOC105369764 ; AQP5
0.925 0.080 12 49965683 upstream gene variant G/A snv 0.55 3
rs2042996
TTN-AS1 ; TTN
0.925 0.080 2 178586693 missense variant G/A snv 0.35 0.35 3
rs2303838
TTN-AS1 ; TTN
0.925 0.080 2 178580212 missense variant C/T snv 0.24 0.24 3
rs2448343
CDK1
0.925 0.080 10 60779886 intron variant A/G;T snv 3
rs2479717
CCND3
0.925 0.080 6 41937436 intron variant T/A snv 0.79 0.81 3
rs249935
PALB2
0.925 0.080 16 23613903 intron variant T/C snv 0.13 3