Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2516049 | 0.742 | 0.400 | 6 | 32602623 | intergenic variant | T/C | snv | 0.27 | 9 | ||
rs477515 | 0.790 | 0.400 | 6 | 32601914 | intergenic variant | G/A | snv | 0.27 | 7 | ||
rs2239804 | 0.851 | 0.240 | 6 | 32443746 | intron variant | T/A;C | snv | 0.51 | 5 | ||
rs2395182 | 0.851 | 0.280 | 6 | 32445540 | downstream gene variant | G/T | snv | 0.76 | 5 | ||
rs7194 | 0.827 | 0.280 | 6 | 32444703 | 3 prime UTR variant | G/A | snv | 0.61 | 5 | ||
rs2227139 | 0.925 | 0.160 | 6 | 32445682 | downstream gene variant | G/A | snv | 0.61 | 4 | ||
rs2239802 | 0.882 | 0.200 | 6 | 32444069 | intron variant | C/A;G;T | snv | 3 | |||
rs2239803 | 0.882 | 0.240 | 6 | 32444056 | intron variant | C/A;T | snv | 0.50 | 3 | ||
rs28366298 | 0.925 | 0.120 | 6 | 32593082 | upstream gene variant | A/C;T | snv | 3 | |||
rs3129888 | 0.882 | 0.240 | 6 | 32443949 | intron variant | G/A | snv | 0.82 | 0.80 | 3 | |
rs2213585 | 1.000 | 0.040 | 6 | 32445373 | downstream gene variant | G/A | snv | 0.61 | 2 | ||
rs2213586 | 1.000 | 0.040 | 6 | 32445317 | downstream gene variant | A/G | snv | 0.61 | 2 | ||
rs7195 | 1.000 | 0.040 | 6 | 32444762 | 3 prime UTR variant | A/G | snv | 0.61 | 2 | ||
rs7754768 | 1.000 | 0.040 | 6 | 32452402 | regulatory region variant | C/T | snv | 0.56 | 2 | ||
rs9268658 | 1.000 | 0.040 | 6 | 32442939 | intron variant | G/A;C | snv | 2 |