Unknown
| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_001146274.1:c.450+33966C>T | 587 | 0.42 | ||
| NM_001146274.1:c.450+31658A>T | 642 | 0.46 | ||
| NM_001146274.1:c.450+29705T>C | 643 | 0.47 | ||
| NM_001146274.1:c.451-10969T>C | 593 | 0.43 | ||
| NM_001146274.1:c.552+9017G>T | 661 | 0.48 | ||
| NM_001146274.1:c.552+1640G>A | 618 | 0.45 | ||
| NM_001146274.1:c.552+7162G>C | 649 | 0.47 |
| Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
|---|---|---|---|---|---|---|
| 125853.G.7.2 | Lebanon | Unknown | Group consisting of 919 control subjects |