Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs171748 | 1.000 | 0.040 | 5 | 61203304 | intron variant | A/G | snv | 0.60 | 2 | ||
rs256377 | 5 | 61210447 | intron variant | A/G | snv | 0.59 | 1 | ||||
rs62366190 | 5 | 61188108 | intron variant | C/G | snv | 0.25 | 1 | ||||
rs159544 | 5 | 61193420 | intron variant | A/C;G | snv | 1 | |||||
rs194369 | 5 | 61203358 | intron variant | A/G | snv | 0.47 | 1 |