Genomics England
GMS Panels
Panels
Genes and Entities
SLC6A6
solute carrier family 6 member 6
OMIM:
186854
See this entity in PanelApp
Panel
Mode of inheritance
Details
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1 panel
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in
Retinal disorders
R-numbers:
R32
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Early retinal degeneration, cardiomyopathy