| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_000594.3:c.-488G>A | 0.0755 | |||
| NG_007462.1:g.4752G>A | 0.0849 | |||
| IL1B (-511) | 0.3726 | |||
| IL1B (+3954) NM_000576.3:c.315C>T | 0.2925 | |||
| NG_016779.1:g.4671T>G | 0.49 | |||
| NM_000586.3:c.114G>T | 0.3168 | |||
| NG_023252.1:g.4272T>G | 0.1971 | |||
| NG_023252.1:g.4782C>T | 0.1619 | |||
| NG_023252.1:g.5338C>T | 0.1238 | |||
| NG_011640.1:g.4880C>G | 0.6442 | |||
| NG_011640.1:g.4456A>G | 0.8173 | |||
| NG_012088.1:g.3943A>G | 0.3679 | |||
| NG_012088.1:g.4206T>C | 0.7028 | |||
| NM_153758.3:c.-35+1984T>G | 0.7184 | |||
| NG_008850.1:g.5012C>T | 0.3538 | |||
| NM_001288706.1:c.-83-12074C>T | 0.3632 | |||
| NM_000577.4:c.336T>C | 0.2358 | |||
| NM_000418.3:c.1727A>G | 0.1762 | |||
| NM_002187.2:c.*159A>C | 0.25 | |||
| NM_000619.2:c.115-483A>T | 0.5 | |||
| NM_000660.4:c.29C>T | 0.601 | |||
| NM_000660.4:c.74G>C | 0.1845 |