For the 20 eQTLs and associated 42 eGenes identified in TCGA but not FH, ZFP57 (paired with rs7767188), TRIM26 (paired with rs7767188), MRM2 (paired with rs527510716), CLDN25 (paired with rs11214775), and ZNF652 (paired with rs11650494) were not available in the FH dataset. The gene discussed is ZNF652; the disease is familial hyperaldosteronism.