Source: BEFREE
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs5219 | 0.701 | 0.360 | 11 | 17388025 | stop gained | T/A;C | snv | 0.64 | 21 | ||
| rs5215 | 0.827 | 0.160 | 11 | 17387083 | missense variant | C/T | snv | 0.64 | 0.71 | 5 | |
| rs80356610 | 0.827 | 0.080 | 11 | 17387968 | missense variant | A/G | snv | 3 | |||
| rs2285676 | 0.925 | 0.120 | 11 | 17386478 | 3 prime UTR variant | A/G | snv | 0.44 | 2 | ||
| rs142577961 | 1.000 | 0.080 | 11 | 17387813 | synonymous variant | G/A | snv | 1.6E-05 | 2.1E-05 | 1 | |
| rs1800467 | 1.000 | 0.080 | 11 | 17387284 | missense variant | G/C;T | snv | 4.0E-02; 2.8E-05 | 1 | ||
| rs41282930 | 1.000 | 0.080 | 11 | 17386938 | missense variant | G/A;C | snv | 4.0E-06; 4.6E-03 | 1 | ||
| rs5210 | 1.000 | 0.080 | 11 | 17386704 | 3 prime UTR variant | G/A;C | snv | 1 | |||
| rs5218 | 1.000 | 0.080 | 11 | 17387522 | synonymous variant | G/A;T | snv | 0.26; 4.1E-06 | 1 | ||
| rs750778014 | 1.000 | 0.080 | 11 | 17387517 | missense variant | C/A;T | snv | 4.0E-06; 8.1E-06 | 1 | ||
| rs774714794 | 1.000 | 0.080 | 11 | 17388012 | missense variant | C/T | snv | 1.6E-05 | 3.5E-05 | 1 |