Unknown
| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_001146274.1:c.450+33966C>T | 639 | 0.35 | ||
| NM_001146274.1:c.450+31658A>T | 694 | 0.38 | ||
| NM_001146274.1:c.450+29705T>C | 709 | 0.39 | ||
| NM_001146274.1:c.451-10969T>C | 613 | 0.33 | ||
| NM_001146274.1:c.552+9017G>T | 650 | 0.35 | ||
| NM_001146274.1:c.552+1640G>A | 741 | 0.40 | ||
| NM_001146274.1:c.552+7162G>C | 856 | 0.47 |
| Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
|---|---|---|---|---|---|---|
| 125853.G.7.1 | Lebanon | Diabetes mellitus | Unknown | Study with 691 T2DM patients |