Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7828135
TPD52
1.000 0.080 8 80146584 intron variant T/C snv 0.12 1
rs116561224 1.000 0.080 18 66962261 intergenic variant A/G snv 7.4E-02 2
rs72631567 1.000 0.080 2 5092045 intergenic variant A/G snv 4.5E-02 2
rs114577328
HLA-A
1.000 0.080 6 29959505 downstream gene variant G/C snv 1.3E-02 2
rs17036170
PPARG
1.000 0.080 3 12288912 5 prime UTR variant G/A snv 1.1E-02 2
rs6139258
RNF24
1.000 0.080 20 3977969 intron variant T/C snv 3.2E-02 2
rs2205986
SYT14
0.925 0.160 1 209942767 intron variant G/A snv 0.92 2
rs9274407
HLA-DQB1
0.925 0.120 6 32665055 missense variant A/C;T snv 0.77 3
rs11012476
NEBL
0.925 0.120 10 21003994 intron variant C/T snv 3.5E-02 3
rs3129900
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32338202 intron variant G/T snv 0.83 3
rs4842407 0.882 0.200 12 78807293 intron variant A/G snv 0.35 4
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 9
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 12