Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9972232 1.000 0.040 14 22269708 intron variant G/A;C snv 1
rs996165
LOC112267867
1.000 0.040 14 22485696 upstream gene variant C/T snv 0.50 1
rs990962 1.000 0.040 14 22099284 downstream gene variant T/C snv 0.16 1
rs979027 1.000 0.040 14 22020269 intergenic variant G/A snv 0.46 1
rs9653226
MYCNOS ; MYCN
0.882 0.080 2 15939632 intron variant C/T snv 0.54 3
rs9404576
HACE1
0.882 0.160 6 104736765 intron variant T/A;G snv 3
rs938050921
DCDC2 ; KAAG1
0.827 0.120 6 24357658 missense variant C/T snv 8.1E-06 5
rs9295536
CASC15
0.882 0.080 6 22131700 intron variant C/A snv 0.58 3
rs915927
XRCC1
0.827 0.120 19 43553075 synonymous variant T/A;C;G snv 0.37 5
rs895459
BARD1
1.000 0.040 2 214735533 intron variant G/A snv 0.34 1
rs879255652
SCN8A
0.807 0.120 12 51790425 stop gained G/A;T snv 7
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs873601
BIVM-ERCC5 ; ERCC5
0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs869312966
SCN8A
0.827 0.120 12 51806345 missense variant G/T snv 7
rs867182279
EGFR
0.882 0.080 7 55205510 missense variant T/C snv 3
rs863225285
ALK
0.851 0.080 2 29209789 missense variant T/G snv 5
rs863225281
ALK
0.776 0.200 2 29220829 missense variant G/C;T snv 12
rs8173
AURKA
0.763 0.240 20 56369735 3 prime UTR variant C/G;T snv 9
rs8022710 1.000 0.040 14 22027789 intergenic variant C/A snv 0.71 1
rs8022578 1.000 0.040 14 22101908 upstream gene variant A/G snv 0.30 1
rs8021297
LOC105370401
1.000 0.040 14 22436073 intron variant T/C snv 0.45 1
rs8020193
LOC112267867 ; LOC105370401
1.000 0.040 14 22470475 intron variant A/C snv 0.43 1
rs80059929
KIF15
0.882 0.080 3 44805230 intron variant T/A snv 3.6E-02 3
rs79977247
TTR
0.776 0.200 18 31592975 missense variant T/C;G snv 9