Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs362272 | 1.000 | 0.120 | 4 | 3233253 | missense variant | G/A;T | snv | 0.29 | 2 | ||
| rs363092 | 1.000 | 0.120 | 4 | 3194302 | intron variant | A/C;T | snv | 0.51 | 2 | ||
| rs6855981 | 1.000 | 0.120 | 4 | 3146549 | intron variant | G/A | snv | 0.34 | 2 | ||
| rs10015979 | 1.000 | 0.120 | 4 | 3107715 | intron variant | A/G | snv | 0.30 | 1 | ||
| rs110501 | 1.000 | 0.120 | 4 | 3223751 | intron variant | T/C | snv | 0.47 | 1 | ||
| rs11731237 | 1.000 | 0.120 | 4 | 3150086 | intron variant | C/T | snv | 0.26 | 1 | ||
| rs1210554604 | 1.000 | 0.120 | 4 | 3131662 | missense variant | G/A | snv | 1 | |||
| rs2071655 | 1.000 | 0.120 | 4 | 3116389 | intron variant | T/A;G | snv | 1 | |||
| rs2269499 | 1.000 | 0.120 | 4 | 3237975 | intron variant | C/T | snv | 0.24 | 1 | ||
| rs2285086 | 1.000 | 0.120 | 4 | 3087532 | intron variant | A/G | snv | 0.48 | 1 | ||
| rs2298969 | 1.000 | 0.120 | 4 | 3184517 | intron variant | A/G;T | snv | 1 | |||
| rs2471347 | 1.000 | 0.120 | 4 | 3042708 | intron variant | G/A | snv | 0.68 | 1 | ||
| rs363066 | 1.000 | 0.120 | 4 | 3134226 | intron variant | T/A;G | snv | 1 | |||
| rs363096 | 1.000 | 0.120 | 4 | 3178294 | splice region variant | T/C | snv | 0.55 | 0.60 | 1 | |
| rs3856973 | 1.000 | 0.120 | 4 | 3078446 | intron variant | G/A;C | snv | 1 | |||
| rs82333 | 1.000 | 0.120 | 4 | 3223662 | intron variant | A/C;G | snv | 1 | |||
| rs916171 | 1.000 | 0.120 | 4 | 3215088 | intron variant | C/G | snv | 0.42 | 0.47 | 1 | |
| rs13102260 | 1.000 | 0.120 | 4 | 3074678 | intron variant | G/A | snv | 0.15 | 1 | ||
| rs1313770 | 1.000 | 0.120 | 4 | 3056082 | intron variant | A/G | snv | 0.57 | 1 | ||
| rs2798296 | 1.000 | 0.120 | 4 | 3060438 | intron variant | A/G | snv | 0.44 | 1 | ||
| rs71180116 | 1.000 | 0.120 | 4 | 3074877 | inframe insertion | GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA/-;GCA;GCAGCA;GCAGCAGCA;GCAGCAGCAGCA;GCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA | delins | 0.14 | 1 |