Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4587207 | 1.000 | 6 | 30799168 | intron variant | A/G | snv | 0.17 | 5 | |||
| rs4713380 | 0.925 | 0.120 | 6 | 30817496 | intron variant | T/C | snv | 0.17 | 5 | ||
| rs4713385 | 0.925 | 0.120 | 6 | 30819816 | intron variant | G/A | snv | 0.17 | 5 | ||
| rs9295924 | 0.925 | 0.120 | 6 | 30814584 | non coding transcript exon variant | G/A | snv | 0.27 | 0.17 | 5 | |
| rs9378109 | 0.925 | 0.120 | 6 | 30806697 | intron variant | C/A | snv | 0.16 | 5 | ||
| rs13198118 | 1.000 | 6 | 30802955 | intron variant | T/G | snv | 0.17 | 4 | |||
| rs2394403 | 1.000 | 6 | 30800092 | intron variant | C/T | snv | 0.17 | 4 | |||
| rs4248149 | 1.000 | 6 | 30799850 | intron variant | T/C | snv | 0.17 | 4 | |||
| rs4483030 | 1.000 | 6 | 30799352 | intron variant | C/T | snv | 0.20 | 4 | |||
| rs4713383 | 1.000 | 6 | 30819464 | intron variant | G/A | snv | 0.17 | 4 | |||
| rs4713389 | 1.000 | 6 | 30822827 | intron variant | G/T | snv | 0.17 | 4 | |||
| rs4947290 | 1.000 | 6 | 30826628 | intron variant | G/A | snv | 0.17 | 4 | |||
| rs6901761 | 1.000 | 6 | 30823021 | intron variant | C/T | snv | 0.17 | 4 | |||
| rs6905957 | 1.000 | 6 | 30798963 | intron variant | A/G;T | snv | 4 | ||||
| rs7749924 | 1.000 | 6 | 30830214 | intron variant | C/T | snv | 0.12 | 4 | |||
| rs7751869 | 1.000 | 6 | 30825537 | intron variant | A/G;T | snv | 4 | ||||
| rs9368644 | 1.000 | 6 | 30829306 | intron variant | C/T | snv | 0.17 | 4 | |||
| rs9380198 | 1.000 | 6 | 30818109 | intron variant | G/T | snv | 0.17 | 4 | |||
| rs9391696 | 1.000 | 6 | 30811009 | intron variant | A/G;T | snv | 4 | ||||
| rs9404974 | 1.000 | 6 | 30808706 | intron variant | T/C | snv | 0.17 | 4 |