| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11558471 | 1.000 | 0.080 | 8 | 117173494 | 3 prime UTR variant | A/G | snv | 0.25 | 5 | ||
| rs11603334 | 1.000 | 0.080 | 11 | 72721940 | 5 prime UTR variant | G/A | snv | 0.12 | 5 | ||
| rs11605924 | 1.000 | 0.080 | 11 | 45851540 | intron variant | A/C | snv | 0.39 | 5 | ||
| rs1183910 | 1.000 | 0.080 | 12 | 120983004 | intron variant | G/A | snv | 0.28 | 5 | ||
| rs12208357 | 1.000 | 0.080 | 6 | 160122116 | missense variant | C/T | snv | 5.2E-02 | 4.9E-02 | 5 | |
| rs1272388614 | 0.851 | 0.080 | 11 | 17395658 | missense variant | C/T | snv | 2.4E-05 | 3.5E-05 | 5 | |
| rs137852787 | 0.882 | 0.080 | 13 | 27924519 | missense variant | G/A | snv | 1.3E-03 | 2.0E-04 | 5 | |
| rs148311934 | 0.827 | 0.080 | 7 | 44149763 | missense variant | C/T | snv | 8.0E-06 | 1.4E-05 | 5 | |
| rs17168486 | 1.000 | 0.080 | 7 | 14858657 | intron variant | C/T | snv | 0.18 | 5 | ||
| rs174455 | 1.000 | 0.080 | 11 | 61888645 | intron variant | G/A;C | snv | 5 | |||
| rs1884614 | 0.882 | 0.080 | 20 | 44351879 | non coding transcript exon variant | C/T | snv | 0.18 | 5 | ||
| rs2233580 | 0.882 | 0.080 | 7 | 127613496 | missense variant | C/T | snv | 8.2E-03 | 2.1E-03 | 5 | |
| rs2250417 | 1.000 | 0.080 | 11 | 112214593 | intron variant | T/C | snv | 0.44 | 5 | ||
| rs2304130 | 1.000 | 0.080 | 19 | 19678719 | splice region variant | A/G | snv | 0.10 | 0.12 | 5 | |
| rs3768321 | 1.000 | 0.080 | 1 | 39570256 | intron variant | G/T | snv | 0.14 | 5 | ||
| rs3786897 | 1.000 | 0.080 | 19 | 33402102 | intron variant | A/G | snv | 0.45 | 5 | ||
| rs3794991 | 1.000 | 0.080 | 19 | 19499787 | intron variant | C/G;T | snv | 7.4E-02 | 5 | ||
| rs3802177 | 1.000 | 0.080 | 8 | 117172786 | 3 prime UTR variant | G/A | snv | 0.24 | 5 | ||
| rs587780345 | 0.851 | 0.080 | 7 | 44150004 | missense variant | C/T | snv | 5 | |||
| rs6499863 | 0.925 | 0.080 | 16 | 56958105 | upstream gene variant | G/A | snv | 0.19 | 5 | ||
| rs753285226 | 0.882 | 0.080 | 20 | 44406084 | missense variant | C/A;T | snv | 4.0E-06 | 5 | ||
| rs7570971 | 1.000 | 0.080 | 2 | 135080336 | intron variant | C/A | snv | 0.61 | 5 | ||
| rs7651090 | 0.925 | 0.080 | 3 | 185795604 | intron variant | A/G | snv | 0.39 | 5 | ||
| rs7944584 | 1.000 | 0.080 | 11 | 47314769 | intron variant | A/T | snv | 0.19 | 5 | ||
| rs8192675 | 0.925 | 0.080 | 3 | 171007094 | intron variant | T/C | snv | 0.42 | 5 |