Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 63 | ||
rs3764261 | 0.732 | 0.280 | 16 | 56959412 | upstream gene variant | C/A | snv | 0.31 | 26 | ||
rs11206510 | 0.763 | 0.240 | 1 | 55030366 | intergenic variant | T/A;C;G | snv | 16 | |||
rs602633 | 0.851 | 0.080 | 1 | 109278889 | downstream gene variant | T/G | snv | 0.63 | 10 | ||
rs8087799 | 0.882 | 0.080 | 18 | 22605468 | regulatory region variant | G/A | snv | 0.43 | 3 | ||
rs1795061 | 1.000 | 0.040 | 1 | 214235937 | intergenic variant | T/C;G | snv | 1 | |||
rs9316871 | 1.000 | 0.040 | 13 | 22287782 | intergenic variant | A/G | snv | 0.22 | 1 | ||
rs1799752 | 0.677 | 0.480 | 17 | 63488529 | intron variant | -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT | delins | 25 | |||
rs77294580 | 1.000 | 0.040 | 17 | 63480396 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
rs12692386 | 0.827 | 0.160 | 2 | 9555777 | 5 prime UTR variant | A/G | snv | 0.72 | 5 | ||
rs1524668 | 0.851 | 0.160 | 2 | 9557243 | upstream gene variant | A/C | snv | 0.64 | 4 | ||
rs5186 | 0.630 | 0.560 | 3 | 148742201 | 3 prime UTR variant | A/C | snv | 0.23 | 0.21 | 38 | |
rs12695895 | 0.925 | 0.040 | 3 | 148725481 | intron variant | C/T | snv | 0.31 | 3 | ||
rs919433 | 0.882 | 0.080 | 2 | 197301841 | intron variant | G/A | snv | 0.38 | 3 | ||
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 47 | |
rs1800469 | 0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 | 78 | ||
rs2043211 | 0.653 | 0.480 | 19 | 48234449 | missense variant | A/T | snv | 0.33 | 0.29 | 29 | |
rs12191786 | 0.851 | 0.120 | 6 | 22004398 | intron variant | C/A;T | snv | 4 | |||
rs3877899 | 0.827 | 0.160 | 5 | 42801166 | missense variant | C/A;T | snv | 4.0E-06; 0.20 | 7 | ||
rs7579 | 0.807 | 0.200 | 5 | 42800706 | 3 prime UTR variant | C/T | snv | 0.31 | 0.26 | 6 | |
rs1799864 | 0.572 | 0.680 | 3 | 46357717 | missense variant | G/A | snv | 0.13 | 0.12 | 68 | |
rs1333049 | 0.614 | 0.520 | 9 | 22125504 | intron variant | G/C | snv | 0.41 | 60 | ||
rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 44 | ||
rs10757274 | 0.701 | 0.320 | 9 | 22096056 | intron variant | A/G | snv | 0.41 | 22 | ||
rs2383207 | 0.695 | 0.280 | 9 | 22115960 | intron variant | A/G | snv | 0.64 | 22 |