This panel is used for clinical indication 'R436 Hereditary alpha tryptasaemia' in the NHS Genomic Medicine Service.

Further information on the testing criteria and any overlapping clinical indications can be found within ( under 'R436 Hereditary alpha tryptasaemia'.

A version of this panel has been signed off under NHS Genomic Medicine Service governance (see 'Latest signed off version' in the panel header information).

This panel will continue to be curated based on external reviews and Genomics England curation. New changes will be reflected in an increase to the minor version of the panel and details of these can be viewed in the 'Panel Activity' page. Periodically, these changes will be reviewed by a NHS Genomic Medicine Service evaluation process. The content that is agreed for the GMS panels will be reflected in an updated signed off version number.

CNVs, STRs and genes encoded by the mitochondrial genome may not be routinely included in the analysis where the panel is NOT delivered by WGS. Please contact your Genomic Laboratory Hub for information regarding specific queries.

1 reviewer

  • Sarah Leigh (Genomics England Curator)

    Group: Other
    Workplace: Other

1 Entities

1 reviewed, 1 green

List Entity Reviews Mode of inheritance Details
1 Entities
Green Green List (high evidence)
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • Expert Review Green
  • gene-checked

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