Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2526358 | 17 | 59865224 | intron variant | A/G | snv | 0.16 | 3 | ||||
rs1292053 | 1.000 | 0.040 | 17 | 59886176 | missense variant | A/G | snv | 0.45 | 0.46 | 2 | |
rs201184664 | 17 | 59873258 | intron variant | -/GT | delins | 2 | |||||
rs1292048 | 17 | 59877710 | intron variant | A/G | snv | 0.46 | 2 | ||||
rs4047777 | 17 | 59882526 | intron variant | A/T | snv | 0.27 | 1 | ||||
rs1292056 | 17 | 59881686 | intron variant | C/G;T | snv | 1 | |||||
rs1292058 | 17 | 59880621 | intron variant | A/C;T | snv | 1 |