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 | ||||
| rs11132388 | 4 | 186298264 | intron variant | T/C;G | snv | 1 | |||||
| rs112477227 | 4 | 186310896 | intron variant | C/A | snv | 9.8E-02 | 1 | ||||
| rs28690003 | 4 | 186303408 | intron variant | G/A | snv | 0.15 | 1 | ||||
| rs28864974 | 4 | 186303240 | intron variant | A/G | snv | 0.22 | 1 | ||||
| rs4613610 | 4 | 186301117 | intron variant | A/C;G | snv | 1 | |||||
| rs6815076 | 4 | 186303404 | intron variant | G/C | snv | 0.19 | 1 | ||||
| rs6824705 | 4 | 186292735 | intron variant | C/G;T | snv | 1 | |||||
| rs6843711 | 4 | 186291799 | intron variant | T/C | snv | 0.90 | 1 |