| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7000921 | 0.925 | 0.080 | 8 | 20535695 | intergenic variant | T/C | snv | 0.30 | 2 | ||
| rs7750963 | 1.000 | 0.080 | 6 | 31303790 | intron variant | A/G | snv | 0.80 | 2 | ||
| rs9366816 | 0.925 | 0.080 | 6 | 33136398 | intron variant | T/C | snv | 0.22 | 2 | ||
| rs10214910 | 1.000 | 0.080 | 6 | 33069898 | intron variant | C/A | snv | 0.23 | 0.32 | 1 | |
| rs10243492 | 1.000 | 0.080 | 7 | 32780825 | intergenic variant | A/G | snv | 0.48 | 1 | ||
| rs1042169 | 1.000 | 0.080 | 6 | 33080909 | missense variant | G/A;T | snv | 0.31; 1.4E-02 | 1 | ||
| rs1042190 | 1.000 | 0.080 | 6 | 33069222 | missense variant | T/C | snv | 0.24 | 0.28 | 1 | |
| rs10484569 | 1.000 | 0.080 | 6 | 33091175 | downstream gene variant | G/A | snv | 5.9E-02 | 1 | ||
| rs10485138 | 1.000 | 0.080 | 6 | 100690714 | intron variant | C/T | snv | 2.5E-02 | 1 | ||
| rs10912564 | 1.000 | 0.080 | 1 | 173201479 | intron variant | C/T | snv | 0.43 | 1 | ||
| rs11089620 | 1.000 | 0.080 | 22 | 21568167 | non coding transcript exon variant | C/G | snv | 0.18 | 1 | ||
| rs112120857 | 1.000 | 0.080 | 22 | 39018377 | missense variant | G/C;T | snv | 5.2E-05; 5.4E-03 | 1 | ||
| rs1126542 | 1.000 | 0.080 | 6 | 33069647 | missense variant | T/A;C;G | snv | 0.24 | 0.28 | 1 | |
| rs1126769 | 1.000 | 0.080 | 6 | 33068658 | missense variant | T/G | snv | 0.24 | 0.29 | 1 | |
| rs11355458 | 1.000 | 0.080 | 9 | 125241510 | upstream gene variant | CC/-;C;CCC;CCCC | delins | 1 | |||
| rs1140763 | 1.000 | 0.080 | 9 | 125235313 | 3 prime UTR variant | G/A;C | snv | 1 | |||
| rs11466004 | 1.000 | 0.080 | 8 | 74029040 | missense variant | C/G;T | snv | 1.3E-02 | 1 | ||
| rs11568695 | 1.000 | 0.080 | 13 | 95044286 | synonymous variant | C/T | snv | 1.2E-02 | 4.7E-02 | 1 | |
| rs11638027 | 1.000 | 0.080 | 15 | 90302268 | intron variant | G/T | snv | 9.9E-02 | 1 | ||
| rs12009 | 1.000 | 0.080 | 9 | 125235024 | 3 prime UTR variant | G/A;T | snv | 0.54 | 1 | ||
| rs12233338 | 1.000 | 0.080 | 21 | 33228611 | upstream gene variant | T/C | snv | 0.21 | 1 | ||
| rs12375841 | 1.000 | 0.080 | 9 | 4850141 | intron variant | T/C | snv | 0.33 | 1 | ||
| rs12484550 | 1.000 | 0.080 | 22 | 21587626 | intron variant | C/T | snv | 0.18 | 1 | ||
| rs12649554 | 1.000 | 0.080 | 4 | 100975519 | regulatory region variant | T/C | snv | 0.65 | 1 | ||
| rs12979680 | 1.000 | 0.080 | 19 | 21691444 | intergenic variant | C/A;T | snv | 1 |