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 | 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 | 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 |