Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs1059513 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 6
rs2236379 0.790 0.160 10 6485181 missense variant G/A snv 0.31 0.30 6
rs12576775 0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs12459419 0.925 0.120 19 51225221 missense variant C/G;T snv 0.31 4
rs1801020 1.000 0.040 5 177409531 5 prime UTR variant A/G snv 0.65 0.67 4
rs3812036 0.925 0.120 5 177386403 intron variant C/T snv 0.23 0.20 4
rs6489785 1.000 0.040 12 120925921 TF binding site variant T/C snv 0.68 3
rs4849121 0.925 0.160 2 110842129 intron variant G/A snv 0.44 3
rs9384713
AK9
0.882 0.080 6 109558038 intron variant G/T snv 0.57 3
rs2239633 0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 3
rs2070676 0.827 0.320 10 133537633 non coding transcript exon variant G/C snv 0.73 3
rs4364959 0.882 0.080 10 21996442 intron variant C/T snv 0.77 3
rs12133576
DR1
1.000 0.040 1 93350843 intron variant A/G snv 0.51 3
rs17056278 0.925 0.040 5 158825430 intron variant C/G snv 5.3E-02 3
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs11574637 0.882 0.200 16 31357553 missense variant T/C snv 0.21 3
rs4374383 0.776 0.200 2 112013193 intron variant A/G snv 0.58 3
rs4969186 1.000 0.040 17 78402323 intron variant G/C snv 0.62 3
rs478093 1.000 0.040 1 119712503 5 prime UTR variant A/G snv 0.73 3
rs11709077 0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02 3