Another report presented that 56% of 2198 HL patients from 491 Palestinian families was genetic, and the top five genes implicated were GJB2, MYO15A, SLC26A4, MYO7A, and CDH23 (22%, 11%, 8.9%, 8.3%, 5%, respectively) with most common variant to be c.35delG in GJB2, c.1001 G > T in SLC26A4, and c.7207 G > T in MYO15A [35]. The gene discussed is MYO7A; the disease is Hodgkins lymphoma.