Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7973450
KRAS
0.882 0.080 12 25208208 3 prime UTR variant A/G snv 0.20 3
rs11247957
LIN28A
0.882 0.080 1 26429683 3 prime UTR variant G/A snv 0.21 3
rs17065417
LIN28B
0.882 0.080 6 104958399 intron variant A/C snv 0.10 3
rs204938
LMO1
0.882 0.080 11 8256650 intron variant C/T snv 0.49 3
rs110420
LMO1 ; LOC105376536
0.882 0.080 11 8231502 intron variant T/C snv 0.42 3
rs204926
LMO1 ; LOC105376536
0.882 0.080 11 8233559 intron variant G/A snv 0.41 3
rs138085133
LOC101928216 ; EXTL1
0.882 0.080 1 26022729 missense variant C/G;T snv 8.4E-04; 4.0E-06 3
rs3750952
LOC105376536 ; LMO1
0.882 0.080 11 8230374 synonymous variant G/C;T snv 0.45; 4.8E-05 3
rs1415224147
MAPKAP1
0.882 0.080 9 125585715 missense variant T/C snv 3
rs1273925499
MAPT
0.882 0.080 17 45991557 missense variant C/G;T snv 4.0E-06 3
rs372572360
MAVS
0.882 0.080 20 3864633 missense variant G/A snv 8.0E-06 3
rs765771575
MET
0.882 0.080 7 116782017 missense variant T/C;G snv 4.0E-06; 4.0E-06 3
rs60226897
MYCN
0.882 0.080 2 15947252 downstream gene variant G/A snv 4.3E-02 3
rs13034994
MYCNOS
0.882 0.080 2 15938513 non coding transcript exon variant A/C;G snv 3
rs9653226
MYCNOS ; MYCN
0.882 0.080 2 15939632 intron variant C/T snv 0.54 3
rs147992979
NTRK3
0.882 0.080 15 88184270 missense variant G/A snv 8.0E-05 4.4E-05 3
rs2302616
ODC1-DT ; ODC1 ; SNORA80B
0.882 0.080 2 10448065 intron variant C/A snv 0.26 3
rs749242026
PTPRD
0.882 0.080 9 8341203 missense variant G/T snv 8.0E-06 3
rs6441201
RSRC1
0.882 0.080 3 158460535 intron variant G/A snv 0.51 3
rs17489363
SNHG31 ; BARD1
0.882 0.080 2 214809617 5 prime UTR variant A/G snv 0.73 0.74 3
rs75183227
TH
0.882 0.080 11 2169790 missense variant C/A snv 3
rs3176752
XPA
0.882 0.080 9 97675205 3 prime UTR variant G/T snv 3.8E-02 2.3E-02 3
rs11103603 0.851 0.080 9 134449754 TF binding site variant T/C snv 0.46 4
rs45511401
ABCC1
0.851 0.120 16 16079375 missense variant G/T snv 3.8E-02 3.6E-02 4
rs377522479
ARHGAP24
0.882 0.080 4 85931021 missense variant C/T snv 2.0E-05 3.5E-05 4