HBA2

hemoglobin subunit alpha 2
OMIM: 141850, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green HBA2 in Hydrops fetalis Level 2: Dysmorphic and congenital abnormality syndromes Version 0.328	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Thalassemia, alpha-, MIM# 604131 Tags SV/CNV
Green HBA2 in Mendeliome Version 1.3499	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Erythrocytosis 7, MIM# 617981 Heinz body anaemia, MIM# 140700 Haemoglobin H disease, deletional and nondeletional, MIM# 613978 Thalassaemia, alpha-, MIM# 604131 Tags SV/CNV
Green HBA2 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category A gene Expert Review Green Phenotypes Thalassemia, alpha
Green HBA2 in Red cell disorders Level 2: Haematological disorders Version 1.33	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Yorkshire and North East GLH NHS GMS Wessex and West Midlands GLH North West GLH London South GLH Phenotypes Thalassemia, alpha-, MIM# 604131 Heinz body anaemia, MIM# 140700 Erythrocytosis 7, MIM# 617981
Green HBA2 in Fetal anomalies Version 1.465	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Expert Review Green Victorian Clinical Genetics Services Phenotypes Thalassaemia, alpha-, 604131 Fetal hydrops
Red HBA2 in Prepair 1000+ Level 2: Screening Version 2.14	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Erythrocytosis 7, MIM# 617981 Heinz body anaemia, MIM# 140700 Haemoglobin H disease, deletional and nondeletional, MIM# 613978 Thalassaemia, alpha-, MIM# 604131 Tags SV/CNV
Amber HBA2 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber BabySeq Category A gene BeginNGS Phenotypes Thalassemia, alpha, MIM#604131 Tags treatable haematological technically challenging