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
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
rs9653226
MYCNOS ; MYCN
0.882 0.080 2 15939632 intron variant C/T snv 0.54 3
rs11994014 0.827 0.200 8 24944767 intergenic variant A/G snv 0.70 5
rs1027702 0.882 0.080 1 161743067 intergenic variant C/T snv 0.51 3
rs4758051 0.882 0.080 11 8217092 intergenic variant G/A snv 0.42 3
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs879255652
SCN8A
0.807 0.120 12 51790425 stop gained G/A;T snv 7
rs104894103
APTX
0.807 0.280 9 32974495 stop gained C/G;T snv 4.0E-06; 1.6E-04 6
rs63750355
CHMP2B
0.827 0.160 3 87253472 stop gained C/T snv 5
rs121964884
AVP
0.851 0.200 20 3083005 stop gained G/A;T snv 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614