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HYDIN2 is a recent duplication (found only in humans) of the HYDIN gene found on 16q22.2. [15] GJA5 has been identified as the gene that is responsible for the phenotypes observed with congenital heart diseases on the 1q21.1 location. In case of a duplication of GJA5 tetralogy of Fallot is more common. In case of a deletion other congenital ...