| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11190302 | 1.000 | 0.080 | 10 | 99873158 | downstream gene variant | C/T | snv | 0.37 | 1 | ||
| rs11613092 | 1.000 | 0.080 | 12 | 118455443 | intergenic variant | C/T | snv | 7.9E-02 | 1 | ||
| rs11622883 | 1.000 | 0.080 | 14 | 94689439 | regulatory region variant | T/A | snv | 0.37 | 1 | ||
| rs2279420 | 1.000 | 0.080 | 10 | 60022189 | downstream gene variant | A/G | snv | 8.8E-02 | 1 | ||
| rs7856774 | 1.000 | 0.080 | 9 | 87110354 | regulatory region variant | T/A;C | snv | 1 | |||
| rs7908652 | 1.000 | 0.080 | 10 | 84032167 | intergenic variant | C/T | snv | 0.57 | 1 | ||
| rs770510230 | 1.000 | 0.080 | 19 | 1058155 | stop gained | G/T | snv | 2.0E-05 | 4.2E-05 | 1 | |
| rs754618480 | 1.000 | 0.080 | 17 | 63477951 | synonymous variant | C/T | snv | 4.1E-06 | 1 | ||
| rs371245265 | 1.000 | 0.080 | 7 | 91940884 | 5 prime UTR variant | CGGCGGCGG/-;CGG;CGGCGG;CGGCGGCGGCGG;CGGCGGCGGCGGCGG;CGGCGGCGGCGGCGGCGG;CGGCGGCGGCGGCGGCGGCGG | delins | 1 | |||
| rs771608420 | 1.000 | 0.080 | 7 | 92001217 | missense variant | C/A;T | snv | 2.0E-05; 8.0E-06 | 1 | ||
| rs4417206 | 1.000 | 0.080 | 10 | 95636713 | intron variant | A/C | snv | 0.28 | 1 | ||
| rs138047593 | 1.000 | 0.080 | 2 | 127050470 | missense variant | T/C | snv | 9.2E-03 | 8.2E-03 | 1 | |
| rs67327804 | 1.000 | 0.080 | 2 | 127069056 | intron variant | A/G | snv | 0.30 | 0.33 | 1 | |
| rs754834233 | 1.000 | 0.080 | 2 | 127059060 | missense variant | G/A | snv | 4.1E-05 | 1 | ||
| rs775494528 | 1.000 | 0.080 | 2 | 127057558 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs116754410 | 1.000 | 0.080 | 6 | 47624205 | missense variant | A/G | snv | 2.1E-03 | 8.3E-03 | 1 | |
| rs7179008 | 1.000 | 0.080 | 15 | 32151722 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs116806486 | 1.000 | 0.080 | 1 | 207523640 | missense variant | A/G | snv | 1.6E-03 | 5.4E-03 | 1 | |
| rs3737002 | 1.000 | 0.080 | 1 | 207587428 | missense variant | C/T | snv | 0.28 | 0.23 | 1 | |
| rs2306402 | 1.000 | 0.080 | 10 | 67175727 | intron variant | C/T | snv | 0.38 | 1 | ||
| rs16923760 | 1.000 | 0.080 | 10 | 66920370 | intron variant | T/C | snv | 0.12 | 1 | ||
| rs1117750 | 1.000 | 0.080 | 7 | 14848793 | intron variant | C/T | snv | 0.10 | 1 | ||
| rs202178565 | 1.000 | 0.080 | 7 | 143398406 | missense variant | G/A | snv | 2.1E-04 | 2.2E-04 | 1 | |
| rs3844508 | 1.000 | 0.080 | 6 | 151818907 | intron variant | A/G | snv | 0.23 | 1 | ||
| rs10197851 | 1.000 | 0.080 | 2 | 10345283 | intron variant | A/G | snv | 0.52 | 1 |