Genomics England
GMS Panels
Panels
Genes and Entities
SLC10A2
solute carrier family 10 member 2
OMIM:
601295
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Panel
Mode of inheritance
Details
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Intestinal failure or congenital diarrhoea
R-numbers:
R331
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
?Bile acid malabsorption, primary, 1, OMIM:613291