BCL9L

Panel	Reviews	Mode of inheritance	Details
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Amber BCL9L in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.430	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Other Literature Expert list Phenotypes Congenital Heart Disease Heterotaxy
Amber BCL9L in Heterotaxy Level 2: Dysmorphic and congenital abnormality syndromes Version 1.36	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Other Literature Expert list Phenotypes Heterotaxy Congenital Heart Disease
Amber BCL9L in Mendeliome Version 1.2374	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Other Expert list Literature Phenotypes Heterotaxy syndrome, MONDO:0018677, BCL9L-related
Amber BCL9L in Fetal anomalies Version 1.314	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Other Literature Expert list Genomics England PanelApp Phenotypes Heterotaxy Congenital Heart Disease

4 panels