causes condition has contributing genetic variation causes molecular phenotype Hemoglobin C Hemoglobin S Sickle Cell Disease-SC HBB, GLU6VAL HBB, GLU6LYS SCD Genotype Hemoglobin Genotype SC Request inclusion into relevant ontology SC Genotype SCDO (Jade Hotchkiss) The genotype when an individual has the Hb C gene from one parent and the Hb S gene from the other. Individuals with Hb SC have similar symptoms to individuals with Hb SS, however, the anemia is less severe. None Haemoglobin Genotype SC beta6Glu>Val/beta6Glu>Lys