Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs4925
GSTO1
0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs156697
GSTO2
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs3731249
CDKN2A
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 23
rs2239633
CEBPE
0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 12
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32 10
rs3731217
CDKN2A
0.763 0.320 9 21984662 intron variant A/C;T snv 10
rs4132601
IKZF1
0.763 0.240 7 50402906 3 prime UTR variant T/G snv 0.25 9
rs10828317
PIP4K2A
0.776 0.280 10 22550699 missense variant T/C snv 9
rs1287276985
VEGFA
0.790 0.200 6 43782020 missense variant T/A;C snv 4.0E-06; 4.0E-06 7.0E-06 7
rs866838052
GSTK1 ; LOC105375545
0.851 0.160 7 143267618 missense variant C/A snv 6
rs62527607
BAALC ; BAALC-AS2
0.827 0.160 8 103141321 non coding transcript exon variant G/T snv 0.14 5
rs11980379
IKZF1
0.882 0.120 7 50402283 3 prime UTR variant T/C snv 0.25 3
rs189434316 0.925 0.120 14 92231568 intergenic variant A/T snv 4.1E-02 2
rs2393732
ARID5B
0.925 0.120 10 62007470 intron variant G/A snv 0.15 2
rs4948488
ARID5B
0.925 0.120 10 61925395 intron variant C/A;T snv 2
rs7090445
ARID5B
0.925 0.120 10 61961417 intron variant C/G;T snv 0.70 2
rs35837782
LHPP
0.925 0.120 10 124604740 intron variant A/G snv 0.63 2
rs28665337
CCDC26
1.000 0.120 8 129181858 intron variant C/A;T snv 1
rs4762284
ELK3
1.000 0.120 12 96218984 intron variant A/T snv 0.36 1