Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs3828805
HLA-DQB1
0.752 0.160 6 32668343 5 prime UTR variant T/A;C snv 12
rs79767424 0.827 0.080 5 19108581 intron variant G/T snv 4.1E-02 7
rs77452476
LAMC3
0.827 0.080 9 131087186 intron variant T/G snv 0.18 7
rs1453414
TRIM5 ; OR52N2
0.827 0.080 11 5807854 intron variant G/C;T snv 7