| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
| rs2471336 | 1.000 | 0.120 | 4 | 2995884 | intron variant | T/C | snv | 0.32 | 1 | ||
| rs2471347 | 1.000 | 0.120 | 4 | 3042708 | intron variant | G/A | snv | 0.68 | 1 | ||
| rs2749782 | 1.000 | 0.120 | 4 | 3338034 | intron variant | T/C | snv | 0.70 | 1 | ||
| rs2798296 | 1.000 | 0.120 | 4 | 3060438 | intron variant | A/G | snv | 0.44 | 1 | ||
| rs2857845 | 1.000 | 0.120 | 4 | 3026386 | intron variant | A/T | snv | 0.11 | 1 | ||
| rs2857861 | 1.000 | 0.120 | 4 | 3322040 | intron variant | C/T | snv | 0.53 | 1 | ||
| rs2960308 | 1.000 | 0.120 | 4 | 2989313 | intron variant | G/A | snv | 0.48 | 1 | ||
| rs3095073 | 1.000 | 0.120 | 4 | 3261411 | missense variant | G/A | snv | 0.33 | 0.33 | 1 | |
| rs3095079 | 1.000 | 0.120 | 4 | 3263687 | intron variant | C/G;T | snv | 1 | |||
| rs3129308 | 1.000 | 0.120 | 4 | 3307545 | intron variant | G/A | snv | 0.66 | 1 | ||
| rs3129319 | 1.000 | 0.120 | 4 | 3263654 | intron variant | A/G | snv | 0.37 | 1 | ||
| rs3135146 | 1.000 | 0.120 | 4 | 3305911 | intron variant | C/A;G;T | snv | 1 | |||
| rs36117895 | 1.000 | 0.120 | 3 | 11358545 | missense variant | T/C | snv | 3.2E-02 | 3.9E-02 | 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 | |||
| rs4523977 | 1.000 | 0.120 | 17 | 41727098 | missense variant | G/A | snv | 0.23 | 0.18 | 1 | |
| rs6446740 | 1.000 | 0.120 | 4 | 3407656 | intron variant | G/A | snv | 0.57 | 1 | ||
| rs704352 | 1.000 | 0.120 | 4 | 2484759 | intron variant | C/A;T | snv | 0.20 | 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 | ||
| rs71358386 | 1.000 | 0.120 | 17 | 16047840 | intron variant | T/C | snv | 4.1E-02 | 1 | ||
| rs73786719 | 1.000 | 0.120 | 6 | 146716848 | intron variant | C/A | snv | 1.7E-02 | 3.3E-02 | 1 |