Direct billirubin of 0.49, indirect level of 1.82. Normal CBC, other liver tests, and Ultrasound for liver. Is this indicative of gilberts syndrome?

Gilbert's disease. It is a familial (autosomal dominant), common (2-5% of people), unconjugated hyperbilirubinemia (blood bilirubin measures 1-5mg/dl), not due to breakdown of blood. It is associated with reduced enzyme levels of udp glycuronyl transferase, that results in jaundice when patients fast or suffer an infection. It does not shorten life or raise insurance rates, but may predispose to tylenol (acetaminophen) toxicity.