Among these variants, five (19.5%) were not found in the ClinVar database: two were harbored by genes with definite association with NSHL (DIAPH1 and GIPC3), one was harbored by a gene with strong association (MYO3A), one had limited association (TBC1D24), and another one was associated with a syndromic form of HL (PHYH). The gene discussed is TBC1D24; the disease is nodular sclerosis classical Hodgkin lymphoma.