Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 157 | |
rs2043211 | 0.653 | 0.480 | 19 | 48234449 | missense variant | A/T | snv | 0.33 | 0.29 | 29 | |
rs7493 | 0.677 | 0.440 | 7 | 95405463 | missense variant | G/C | snv | 0.27 | 0.27 | 24 | |
rs17128183 | 0.882 | 0.120 | 14 | 55112795 | intergenic variant | A/G | snv | 0.57 | 5 | ||
rs2274273 | 0.882 | 0.120 | 14 | 55147918 | downstream gene variant | G/A | snv | 0.40 | 5 | ||
rs769665945 | 0.882 | 0.160 | 7 | 101137079 | missense variant | C/A;T | snv | 4.0E-06; 3.6E-05 | 3 |