Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs7504990
DCC
0.851 0.120 18 52991406 intron variant T/C snv 0.73 4
rs975334
CNTN4
0.925 0.080 3 2804632 intron variant G/A snv 0.50 2
rs17209837 1.000 0.080 7 87495506 intergenic variant T/C snv 0.19 1
rs1558375
ABCB4
1.000 0.080 7 87449753 intron variant T/C snv 0.27 1
rs117856857
MYC ; CASC11
1.000 0.080 8 127736248 missense variant C/G snv 1.7E-02 1