Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4444878 | 0.851 | 0.120 | 4 | 186292729 | intron variant | C/A;T | snv | 7 | |||
| rs2289252 | 1.000 | 0.040 | 4 | 186286227 | non coding transcript exon variant | C/T | snv | 0.35 | 4 | ||
| rs10025152 | 4 | 186304150 | intron variant | G/A | snv | 0.20 | 2 | ||||
| rs10029715 | 4 | 186301446 | intron variant | T/C | snv | 0.22 | 2 | ||||
| rs1008728 | 4 | 186305519 | intron variant | C/T | snv | 0.57 | 2 | ||||
| rs12500826 | 4 | 186306297 | intron variant | T/C | snv | 0.60 | 2 | ||||
| rs4572916 | 4 | 186302429 | intron variant | A/C | snv | 0.22 | 2 | ||||
| rs907439 | 4 | 186299593 | intron variant | C/T | snv | 0.14 | 2 | ||||
| rs11132387 | 4 | 186297569 | intron variant | G/A;C | snv | 1 | |||||
| rs149130695 | 4 | 186464194 | intron variant | A/C | snv | 5.0E-02 | 1 |