HBG2, hemoglobin subunit gamma 2, 3048

N. diseases: 112; N. variants: 42
Disease: Anemia, Sickle Cell ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7948471
rs7948471
Entrez Id: 3046;3048;282763;390064
Gene Symbol: HBE1;HBG2;OR51B5;OR51I2
HBE1;HBG2;OR51B5;OR51I2
CUI: C0002895
Disease:
Anemia, Sickle Cell 		A 0.700 GeneticVariation GWASCAT Genetic determinants of haemolysis in sickle cell anaemia. 23406172 2013