| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | ||
| rs10934657 | 1.000 | 0.120 | 3 | 124093989 | intron variant | T/C | snv | 0.60 | 1 | ||
| rs1232027 | 1.000 | 0.120 | 5 | 80619201 | intron variant | G/A | snv | 0.32 | 1 | ||
| rs2234759 | 1.000 | 0.120 | 4 | 155208405 | non coding transcript exon variant | A/C;G | snv | 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 | |||
| rs3129319 | 1.000 | 0.120 | 4 | 3263654 | intron variant | A/G | snv | 0.37 | 1 | ||
| rs71358386 | 1.000 | 0.120 | 17 | 16047840 | intron variant | T/C | snv | 4.1E-02 | 1 | ||
| rs12641989 | 1.000 | 0.120 | 4 | 3418113 | non coding transcript exon variant | G/A;C | snv | 1 | |||
| rs16844309 | 1.000 | 0.120 | 4 | 3416539 | intron variant | G/A | snv | 0.26 | 1 | ||
| rs1730768 | 1.000 | 0.120 | 4 | 3407632 | intron variant | A/G | snv | 0.85 | 1 | ||
| rs2749782 | 1.000 | 0.120 | 4 | 3338034 | intron variant | T/C | snv | 0.70 | 1 | ||
| rs2857861 | 1.000 | 0.120 | 4 | 3322040 | intron variant | C/T | snv | 0.53 | 1 | ||
| rs3129308 | 1.000 | 0.120 | 4 | 3307545 | intron variant | G/A | snv | 0.66 | 1 | ||
| rs3135146 | 1.000 | 0.120 | 4 | 3305911 | intron variant | C/A;G;T | snv | 1 | |||
| rs6446740 | 1.000 | 0.120 | 4 | 3407656 | intron variant | G/A | snv | 0.57 | 1 | ||
| rs7435601 | 1.000 | 0.120 | 4 | 3367918 | intron variant | T/C | snv | 0.70 | 1 | ||
| rs11248108 | 1.000 | 0.120 | 4 | 2479763 | intron variant | G/A;T | snv | 1 | |||
| rs704352 | 1.000 | 0.120 | 4 | 2484759 | intron variant | C/A;T | snv | 0.20 | 1 | ||
| rs10937921 | 1.000 | 0.120 | 4 | 3274764 | downstream gene variant | C/T | snv | 0.40 | 2 |