| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10159239 | 0.882 | 0.040 | 1 | 247443750 | intron variant | G/A | snv | 0.57 | 3 | ||
| rs1051339 | 0.882 | 0.040 | 10 | 89247582 | missense variant | C/T | snv | 9.5E-02 | 0.13 | 3 | |
| rs10918859 | 0.882 | 0.040 | 1 | 162199478 | intron variant | G/A | snv | 0.16 | 3 | ||
| rs12040273 | 0.882 | 0.040 | 1 | 230063651 | intron variant | C/T | snv | 0.28 | 3 | ||
| rs12115090 | 0.882 | 0.040 | 8 | 75012585 | intron variant | A/C | snv | 0.33 | 0.44 | 3 | |
| rs12344245 | 0.882 | 0.040 | 9 | 69340801 | intron variant | A/G | snv | 0.12 | 3 | ||
| rs12704673 | 0.882 | 0.040 | 7 | 93525009 | intron variant | A/G;T | snv | 0.27 | 3 | ||
| rs1351855165 | 0.882 | 0.040 | 15 | 45111550 | synonymous variant | G/A | snv | 3 | |||
| rs138760780 | 0.882 | 0.040 | 1 | 205515245 | intron variant | C/T | snv | 1.5E-02 | 3 | ||
| rs1411364031 | 0.882 | 0.040 | 6 | 31577502 | missense variant | T/C | snv | 7.0E-06 | 3 | ||
| rs141383962 | 0.882 | 0.040 | 8 | 27605112 | missense variant | C/G;T | snv | 7.2E-05 | 1.0E-04 | 3 | |
| rs1433748662 | 0.882 | 0.040 | 2 | 8791221 | missense variant | T/C | snv | 3 | |||
| rs145297799 | 0.882 | 0.040 | 7 | 44539181 | stop gained | G/A | snv | 9.1E-05 | 9.8E-05 | 3 | |
| rs16941382 | 0.882 | 0.040 | 17 | 46966142 | intron variant | T/C | snv | 0.15 | 3 | ||
| rs16998248 | 0.882 | 0.040 | 20 | 53581801 | synonymous variant | T/A | snv | 0.11 | 8.8E-02 | 3 | |
| rs189970623 | 0.882 | 0.040 | 19 | 41009368 | missense variant | C/A;G;T | snv | 3.0E-04 | 3 | ||
| rs2254638 | 0.882 | 0.040 | 21 | 28883961 | intron variant | A/C;G | snv | 3 | |||
| rs2267788 | 0.882 | 0.040 | 16 | 9794742 | intron variant | C/T | snv | 3 | |||
| rs2870463 | 0.882 | 0.040 | 16 | 75216819 | upstream gene variant | G/A | snv | 0.14 | 3 | ||
| rs3045215 | 0.882 | 0.040 | 1 | 234605171 | 3 prime UTR variant | -/GTTACAATA;GTTATAATA | delins | 3 | |||
| rs321159 | 0.882 | 0.040 | 17 | 32628611 | intron variant | A/G;T | snv | 3 | |||
| rs352493 | 0.882 | 0.040 | 19 | 4180839 | missense variant | C/G;T | snv | 0.88 | 3 | ||
| rs35511654 | 0.882 | 0.040 | 1 | 111500165 | missense variant | T/G | snv | 9.4E-02 | 9.8E-02 | 3 | |
| rs35720349 | 0.882 | 0.040 | 20 | 53577121 | missense variant | G/A | snv | 3.4E-02 | 1.6E-02 | 3 | |
| rs371150372 | 0.882 | 0.040 | 2 | 27223972 | missense variant | G/A;T | snv | 2.8E-05; 4.0E-06 | 3 |