Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12466865 | 2 | 64655280 | intron variant | C/T | snv | 0.30 | 2 | ||||
rs140625215 | 2 | 64632896 | 3 prime UTR variant | TTCAAA/- | delins | 0.26 | 2 | ||||
rs6753848 | 2 | 64723661 | intron variant | C/G;T | snv | 2 | |||||
rs12471768 | 2 | 64701469 | intron variant | T/C;G | snv | 1 | |||||
rs2160348 | 2 | 64682032 | intron variant | T/C | snv | 0.68 | 1 | ||||
rs3755189 | 2 | 64654863 | intron variant | G/A | snv | 0.35 | 1 |