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
rs8181047
CDKN2B-AS1
0.807 0.120 9 22064466 intron variant A/G snv 0.79 7
rs6547741
GPN1
0.807 0.080 2 27633057 intron variant G/A snv 0.53 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
rs1800628 0.827 0.080 6 31579073 downstream gene variant G/A snv 7.3E-02 6
rs3129780 0.827 0.080 6 32679924 intergenic variant T/A;C snv 6
rs10462706
CLPTM1L
0.827 0.080 5 1343679 intron variant C/T snv 0.14 6
rs928674
LAMC3
0.827 0.080 9 131076637 intron variant A/G snv 0.16 6
rs10851478
LOC105370811 ; FAM227B
0.827 0.080 15 49536822 intron variant T/C snv 0.30 6
rs2398180
NR2F2-AS1
0.827 0.080 15 96319940 intron variant C/T snv 0.62 6