Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28730839 | 17 | 63483140 | missense variant | C/A;G | snv | 4.0E-06; 4.8E-04 | 2 | ||||
rs4329 | 17 | 63486097 | intron variant | A/C;G | snv | 2 | |||||
rs4343 | 0.742 | 0.480 | 17 | 63488670 | synonymous variant | G/A | snv | 0.53 | 1 | ||
rs4351 | 0.925 | 0.160 | 17 | 63492371 | intron variant | G/A | snv | 0.50 | 1 |