MYO15A and Hodgkins lymphoma: Following identification of the c.5492G>T variation in family TAR1, we screened a collective of patients of Turkish origin with recessive inheritance or sporadic incidence of bilateral congenital HL for variations in the GJB2 gene and for the Myo15a c.5492G>T allele to estimate the frequency of this variant in a HL cohort with a Turkish ancestral background (Table 1).