Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs110420
LMO1 ; LOC105376536
0.882 0.080 11 8231502 intron variant T/C snv 0.42 3
rs12442054 0.882 0.080 15 74165683 intron variant G/A snv 0.12 3
rs17065417
LIN28B
0.882 0.080 6 104958399 intron variant A/C snv 0.10 3
rs17251
TRBV27
0.925 0.120 7 142715462 intron variant C/A snv 0.33 0.37 3
rs17487792
BARD1
0.882 0.080 2 214778776 intron variant C/T snv 0.16 3
rs204926
LMO1 ; LOC105376536
0.882 0.080 11 8233559 intron variant G/A snv 0.41 3
rs204938
LMO1
0.882 0.080 11 8256650 intron variant C/T snv 0.49 3
rs2302616
ODC1-DT ; ODC1 ; SNORA80B
0.882 0.080 2 10448065 intron variant C/A snv 0.26 3
rs2619046
DDX4
0.882 0.080 5 55801706 intron variant G/A snv 0.34 3
rs3768707
BARD1
0.882 0.080 2 214780411 intron variant A/G snv 0.74 3
rs3796725
CPZ ; GPR78
0.882 0.080 4 8616210 intron variant C/T snv 0.23 3
rs3796727
GPR78 ; CPZ
0.882 0.080 4 8611299 intron variant G/A snv 0.26 0.32 3
rs4712653
CASC15
0.882 0.080 6 22125735 intron variant T/C;G snv 3
rs6441201
RSRC1
0.882 0.080 3 158460535 intron variant G/A snv 0.51 3
rs80059929
KIF15
0.882 0.080 3 44805230 intron variant T/A snv 3.6E-02 3
rs9295536
CASC15
0.882 0.080 6 22131700 intron variant C/A snv 0.58 3
rs9404576
HACE1
0.882 0.160 6 104736765 intron variant T/A;G snv 3
rs9653226
MYCNOS ; MYCN
0.882 0.080 2 15939632 intron variant C/T snv 0.54 3
rs10131293
LOC105370401
1.000 0.040 14 22461166 intron variant G/A snv 0.15 1
rs10132733
LOC105370401 ; LOC112267867
1.000 0.040 14 22477241 intron variant A/G snv 0.19 1
rs10142552
LOC105370401
1.000 0.040 14 22395232 intron variant G/A snv 3.5E-02 1
rs10148895 1.000 0.040 14 22254840 intron variant C/T snv 0.18 1
rs10162417
LOC105370401
1.000 0.040 14 22460708 intron variant T/G snv 0.15 1
rs1040303
LOC105370401
1.000 0.040 14 22403377 intron variant G/A snv 0.13 1
rs10483273
LOC105370401
1.000 0.040 14 22448054 intron variant A/G snv 9.5E-02 1