| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28903090 | 0.925 | 0.120 | 5 | 132587981 | missense variant | G/T | snv | 1.2E-03 | 1.4E-03 | 2 | |
| rs4725443 | 0.925 | 0.120 | 7 | 152170176 | intron variant | T/C | snv | 9.3E-02 | 2 | ||
| rs56161233 | 0.925 | 0.120 | 2 | 235055489 | 3 prime UTR variant | C/T | snv | 0.11 | 2 | ||
| rs6943984 | 0.925 | 0.120 | 7 | 152201919 | intron variant | G/A | snv | 0.11 | 2 | ||
| rs748148861 | 0.925 | 0.120 | 6 | 167136856 | missense variant | G/C | snv | 8.0E-06 | 2 | ||
| rs865789884 | 0.925 | 0.120 | 8 | 23145778 | missense variant | G/A;C | snv | 4.0E-06 | 2 | ||
| rs1216411295 | 1.000 | 0.120 | 10 | 6025837 | missense variant | A/T | snv | 4.0E-06 | 1 | ||
| rs1378286181 | 1.000 | 0.120 | 19 | 1632076 | missense variant | C/G | snv | 7.0E-06 | 1 | ||
| rs142863665 | 1.000 | 0.120 | 7 | 102111708 | missense variant | G/A | snv | 3.2E-05 | 1.3E-04 | 1 | |
| rs202096899 | 1.000 | 0.120 | 9 | 15489993 | missense variant | C/G;T | snv | 4.5E-05; 4.5E-06 | 5.6E-05 | 1 | |
| rs758417636 | 1.000 | 0.120 | 12 | 6330272 | missense variant | T/C | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs771176824 | 1.000 | 0.120 | 7 | 101916181 | missense variant | C/A;T | snv | 1 | |||
| rs777176672 | 1.000 | 0.120 | 1 | 46066104 | missense variant | T/C | snv | 8.0E-06 | 1 | ||
| rs1321311 | 0.742 | 0.160 | 6 | 36655123 | regulatory region variant | C/A | snv | 0.28 | 15 | ||
| rs1665650 | 0.752 | 0.160 | 10 | 116727589 | intron variant | T/C | snv | 0.69 | 12 | ||
| rs59336 | 0.776 | 0.160 | 12 | 114678547 | intron variant | T/A;G | snv | 0.49 | 10 | ||
| rs2230600 | 0.827 | 0.160 | 4 | 86769845 | missense variant | A/G | snv | 0.18 | 0.14 | 5 | |
| rs5744455 | 0.882 | 0.160 | 5 | 140633722 | upstream gene variant | G/A;T | snv | 5 | |||
| rs11191865 | 0.925 | 0.160 | 10 | 103913084 | intron variant | G/A | snv | 0.44 | 3 | ||
| rs10088262 | 0.925 | 0.160 | 8 | 123753462 | intergenic variant | A/G | snv | 0.56 | 2 | ||
| rs12765878 | 0.925 | 0.160 | 10 | 103909864 | intron variant | T/A;C | snv | 2 | |||
| rs937283 | 0.716 | 0.200 | 12 | 68808384 | 5 prime UTR variant | A/G | snv | 0.37 | 19 | ||
| rs115160714 | 0.807 | 0.200 | 3 | 133601021 | 3 prime UTR variant | G/A | snv | 5.8E-03 | 9 | ||
| rs769412 | 0.851 | 0.200 | 12 | 68839435 | synonymous variant | A/G | snv | 5.5E-02 | 7.5E-02 | 6 | |
| rs9363918 | 0.882 | 0.200 | 6 | 68432116 | intron variant | T/G | snv | 0.38 | 3 |