| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_000594.3:c.-488G>A | 25 | 0.15 | ||
| IL1B (+3954) NM_000576.3:c.315C>T | 47 | 0.36 | ||
| NM_000619.2:c.115-483A>T | 71 | 0.46 | ||
| NM_000660.4:c.29C>T | 71 | 0.51 | ||
| NM_000660.4:c.74G>C | 11 | 0.08 | ||
| NM_001178130.2:c.-382A>G | 83 | 0.58 |
| Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
|---|---|---|---|---|---|---|
| 145500.G.10.2 | United Arab Emirates | 72 normotensives |