| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11515 | 0.882 | 0.040 | 9 | 21968200 | 3 prime UTR variant | C/A;G | snv | 4.0E-06; 0.88 | 6 | ||
| rs3731249 | 0.683 | 0.320 | 9 | 21970917 | missense variant | C/A;G;T | snv | 2.1E-02 | 23 | ||
| rs45456595 | 9 | 21974641 | missense variant | C/G | snv | 2.0E-03 | 2.1E-03 | 1 | |||
| rs6413464 | 1.000 | 0.040 | 9 | 21970980 | missense variant | C/A;G | snv | 1.3E-03; 4.1E-06 | 2 | ||
| rs199907548 | 0.882 | 0.160 | 9 | 21974682 | missense variant | A/C;G | snv | 6.3E-04 | 5 | ||
| rs116150891 | 1.000 | 0.040 | 9 | 21970929 | missense variant | G/A;C | snv | 5.6E-04 | 2.6E-03 | 1 | |
| rs6413463 | 1.000 | 0.040 | 9 | 21970990 | missense variant | A/G;T | snv | 2.9E-05; 3.0E-04 | 1 | ||
| rs587780668 | 0.925 | 0.120 | 9 | 21974796 | start lost | GGCTCCATGCTGCTCCCCGCCGCC/-;GGCTCCATGCTGCTCCCCGCCGCCGGCTCCATGCTGCTCCCCGCCGCC | delins | 1.5E-04 | 3 | ||
| rs372266620 | 0.925 | 0.120 | 9 | 21971189 | missense variant | G/A;C;T | snv | 9.1E-05; 2.3E-05; 9.1E-06 | 2 | ||
| rs200863613 | 0.925 | 0.080 | 9 | 21971061 | missense variant | C/A;T | snv | 8.5E-05 | 3.7E-04 | 6 | |
| rs1800586 | 0.851 | 0.240 | 9 | 21974861 | 5 prime UTR variant | C/A;G;T | snv | 4.3E-05; 6.1E-05; 8.7E-06 | 5 | ||
| rs550846229 | 1.000 | 0.040 | 9 | 21974658 | missense variant | G/A;C | snv | 5.2E-05 | 1 | ||
| rs779306249 | 1.000 | 0.120 | 9 | 21994234 | frameshift variant | -/C | delins | 1.7E-05 | 1.4E-05 | 1 | |
| rs1287464120 | 1.000 | 0.120 | 9 | 21994235 | stop gained | C/A;T | snv | 1.7E-05 | 1 | ||
| rs104894097 | 0.807 | 0.240 | 9 | 21974757 | missense variant | C/A;G;T | snv | 1.7E-05; 1.3E-05 | 8 | ||
| rs770859592 | 1.000 | 0.080 | 9 | 21974599 | missense variant | C/T | snv | 1.6E-05 | 1.4E-05 | 1 | |
| rs759763964 | 0.925 | 0.120 | 9 | 21971142 | missense variant | C/G;T | snv | 1.4E-05 | 2 | ||
| rs1277299943 | 9 | 21974817 | missense variant | G/C | snv | 1.3E-05 | 1 | ||||
| rs768966657 | 1.000 | 0.120 | 9 | 21971021 | inframe insertion | -/ACG | delins | 1.3E-05 | 2 | ||
| rs746834149 | 1.000 | 9 | 21974724 | missense variant | C/A;G;T | snv | 4.1E-06; 1.2E-05 | 1 | |||
| rs372670098 | 9 | 21971153 | missense variant | T/C | snv | 9.5E-06 | 2.8E-05 | 1 | |||
| rs771138120 | 0.827 | 0.120 | 9 | 21971191 | missense variant | G/A;C;T | snv | 9.1E-06; 4.5E-06 | 13 | ||
| rs104894095 | 0.827 | 0.120 | 9 | 21971200 | missense variant | C/G;T | snv | 9.0E-06 | 6 | ||
| rs878853646 | 0.882 | 0.080 | 9 | 21971106 | missense variant | C/A;T | snv | 4.3E-06; 8.6E-06 | 3 | ||
| rs749714198 | 0.882 | 0.200 | 9 | 21971100 | missense variant | G/A | snv | 8.6E-06 | 7.0E-06 | 4 |