| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2733201 | 0.925 | 0.040 | 15 | 44116203 | intron variant | T/A;C | snv | 2 | |||
| rs35610040 | 1.000 | 0.040 | 20 | 23635832 | intron variant | T/C | snv | 0.19 | 2 | ||
| rs4357117 | 0.925 | 0.040 | 6 | 66873865 | intergenic variant | G/T | snv | 1.7E-02 | 2 | ||
| rs57578064 | 0.925 | 0.040 | 9 | 37590253 | intron variant | G/A | snv | 1.9E-02 | 2 | ||
| rs62568141 | 0.925 | 0.040 | 9 | 77012344 | regulatory region variant | C/T | snv | 2.4E-02 | 2 | ||
| rs9295128 | 0.925 | 0.040 | 6 | 160330499 | intergenic variant | G/T | snv | 1.1E-02 | 2 | ||
| rs113681054 | 1.000 | 0.040 | 12 | 21250045 | intergenic variant | T/C | snv | 0.18 | 1 | ||
| rs117038461 | 1.000 | 0.040 | 7 | 100243731 | intron variant | C/T | snv | 1.5E-02 | 1 | ||
| rs1235324522 | 1.000 | 0.040 | 5 | 76732662 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs140104968 | 1.000 | 0.040 | 7 | 99946004 | intron variant | C/T | snv | 1.5E-02 | 1 | ||
| rs140607780 | 1.000 | 0.040 | 7 | 100505900 | upstream gene variant | G/A | snv | 1.0E-02 | 1 | ||
| rs147642358 | 1.000 | 0.040 | 7 | 99335136 | intron variant | G/A;T | snv | 1 | |||
| rs1776964 | 1.000 | 0.040 | 20 | 4899662 | synonymous variant | G/A | snv | 0.47 | 0.45 | 1 | |
| rs188845491 | 1.000 | 0.040 | 7 | 99689016 | intron variant | C/T | snv | 2.5E-04 | 1 | ||
| rs61361928 | 1.000 | 0.040 | 4 | 69096657 | missense variant | T/C | snv | 2.6E-03 | 2.8E-03 | 1 | |
| rs6139591 | 1.000 | 0.040 | 20 | 4970713 | intron variant | G/A | snv | 0.40 | 1 | ||
| rs62471956 | 1.000 | 0.040 | 7 | 99823462 | upstream gene variant | G/A | snv | 3.4E-02 | 1 | ||
| rs747112750 | 1.000 | 0.040 | 1 | 202307363 | synonymous variant | C/T | snv | 4.0E-06 | 1 | ||
| rs7528419 | 0.851 | 0.080 | 1 | 109274570 | 3 prime UTR variant | A/G | snv | 0.23 | 13 | ||
| rs12149545 | 0.851 | 0.080 | 16 | 56959249 | upstream gene variant | G/A | snv | 0.23 | 7 | ||
| rs11635252 | 0.925 | 0.080 | 15 | 90528542 | upstream gene variant | T/C | snv | 0.88 | 4 | ||
| rs117714106 | 0.882 | 0.080 | 14 | 84338144 | intergenic variant | C/T | snv | 9.1E-03 | 3 | ||
| rs1967309 | 0.925 | 0.080 | 16 | 4015582 | non coding transcript exon variant | A/G | snv | 0.51 | 3 | ||
| rs201052613 | 0.882 | 0.080 | 1 | 173026503 | intron variant | T/-;TT | delins | 9.4E-03 | 3 | ||
| rs5940 | 0.882 | 0.080 | 2 | 187466977 | missense variant | C/T | snv | 1.3E-02 | 1.4E-02 | 3 |