Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 7
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 6
rs4842407 0.882 0.200 12 78807293 intron variant A/G snv 0.35 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
rs9274407
HLA-DQB1
0.925 0.120 6 32665055 missense variant A/C;T snv 0.77 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
rs10812428 1.000 0.080 9 26614849 intergenic variant C/T snv 0.40 1
rs113206698 1.000 0.080 10 92818147 intergenic variant G/A snv 2.6E-02 1
rs114811931 1.000 0.080 5 161257724 intergenic variant T/C snv 1.8E-02 1
rs116561224 1.000 0.080 18 66962261 intergenic variant A/G snv 7.4E-02 1
rs116606120 1.000 0.080 5 28665845 intron variant T/A snv 1.0E-02 1
rs149014830 1.000 0.080 5 121540642 intergenic variant C/A;G snv 1.3E-02 1
rs186920977 1.000 0.080 2 56422795 intergenic variant G/A snv 1.1E-02 1
rs2523822 1.000 0.080 6 29860883 intron variant A/G snv 0.26 1
rs61858823 1.000 0.080 10 65095495 intergenic variant G/A snv 1.3E-02 1
rs6582630 1.000 0.080 12 38349706 intergenic variant G/A snv 0.62 1
rs6694270 1.000 0.080 1 18793883 intergenic variant A/G snv 0.26 1
rs72631567 1.000 0.080 2 5092045 intergenic variant A/G snv 4.5E-02 1
rs72696020 1.000 0.080 14 88105563 intergenic variant G/A snv 9.9E-03 1
rs117491755
ASTN2
1.000 0.080 9 116881377 intron variant A/C snv 2.6E-02 1
rs10404821
C19orf81
1.000 0.080 19 50657831 intron variant C/A;T snv 1
rs185305928
CAMTA1
1.000 0.080 1 6845651 intron variant G/A snv 9.3E-03 1