| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12478234 | 1.000 | 0.040 | 2 | 179470242 | intron variant | G/A | snv | 0.15 | 1 | ||
| rs11598767 | 1.000 | 0.040 | 10 | 62421587 | intron variant | T/C | snv | 3.0E-02 | 2 | ||
| rs7915131 | 1.000 | 0.040 | 10 | 62658896 | non coding transcript exon variant | C/T | snv | 0.53 | 1 | ||
| rs73416724 | 1.000 | 0.040 | 6 | 43370064 | non coding transcript exon variant | A/G | snv | 0.11 | 2 | ||
| rs13195040 | 1.000 | 0.040 | 6 | 27446145 | downstream gene variant | A/G | snv | 9.0E-02 | 2 | ||
| rs1233710 | 1.000 | 0.040 | 6 | 28247668 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs17720293 | 1.000 | 0.040 | 6 | 28246920 | intron variant | C/T | snv | 6.4E-02 | 7.2E-02 | 1 | |
| rs2235359 | 0.925 | 0.160 | 6 | 28247863 | intron variant | T/G | snv | 0.20 | 1 | ||
| rs6921919 | 1.000 | 0.040 | 6 | 28357424 | intron variant | C/G | snv | 0.23 | 2 | ||
| rs9297357 | 0.851 | 0.040 | 8 | 105130105 | intron variant | C/G;T | snv | 5 | |||
| rs1460583 | 1.000 | 0.040 | 8 | 105096365 | intron variant | T/C | snv | 0.26 | 1 | ||
| rs385492 | 1.000 | 0.040 | 6 | 29681770 | upstream gene variant | T/C | snv | 0.57 | 2 | ||
| rs201061212 | 1.000 | 0.040 | 15 | 80091637 | intron variant | AAAA/-;AA;AAA | delins | 4.3E-05 | 1 | ||
| rs6707588 | 1.000 | 0.040 | 2 | 219196879 | intron variant | T/C | snv | 0.61 | 1 | ||
| rs12991836 | 1.000 | 0.040 | 2 | 144383974 | intron variant | A/C;T | snv | 2 | |||
| rs17687067 | 1.000 | 0.040 | 8 | 17178692 | intron variant | A/C | snv | 0.17 | 1 | ||
| rs4843613 | 0.925 | 0.040 | 16 | 87456092 | intron variant | T/C | snv | 0.66 | 2 | ||
| rs9841504 | 0.827 | 0.120 | 3 | 114643917 | intron variant | C/G;T | snv | 3 | |||
| rs116663187 | 1.000 | 0.040 | 6 | 28610509 | intron variant | A/G | snv | 2 | |||
| rs115031589 | 1.000 | 0.040 | 6 | 28594812 | intron variant | G/A | snv | 1 | |||
| rs2961033 | 1.000 | 0.040 | 7 | 76335026 | intron variant | T/C | snv | 0.17 | 1 | ||
| rs56007784 | 1.000 | 0.040 | 17 | 1387656 | intron variant | C/G | snv | 0.37 | 1 | ||
| rs149776388 | 1.000 | 0.040 | 8 | 11008861 | intron variant | C/A;T | snv | 1 | |||
| rs149268645 | 0.882 | 0.040 | 2 | 202968295 | intron variant | G/A | snv | 8.4E-02 | 4 | ||
| rs7558283 | 1.000 | 0.040 | 2 | 214424561 | intron variant | T/C | snv | 0.56 | 2 |