Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28530648 | 1.000 | 0.120 | 6 | 32559302 | intron variant | A/C;T | snv | 1 | |||
rs4937362 | 0.827 | 0.240 | 11 | 128622844 | intron variant | T/C | snv | 0.49 | 1 | ||
rs2894253 | 1.000 | 0.120 | 6 | 32377763 | intron variant | T/G | snv | 1.0E-01 | 1 | ||
rs1493202 | 1.000 | 0.120 | 8 | 70993352 | intron variant | T/G | snv | 0.41 | 1 |