HBG2, hemoglobin subunit gamma 2, 3048

N. diseases: 112; N. variants: 42
Disease: Congenital Methemoglobinemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35103459
rs35103459
Entrez Id: 3048
Gene Symbol: HBG2
HBG2
CUI: C0272087
Disease:
Congenital Methemoglobinemia 		0.010 GeneticVariation BEFREE Hereditary methemoglobinemia caused by Hb M-Hyde Park (Hb M-Akita) (HBB:c.277C > T; p.His93Tyr). 31267164 2019