DECIPHER is used by the clinical community to share and compare phenotypic and genotypic data. The DECIPHER database contains data from 51,828 patients who have given consent …

This is a list of genes for which DECIPHER has open-access patient sequence variants, or DDD research sequence variants. These pages contain information about the genes and their …

DECIPHER helps the clinical community share and compare human genome variants and phenotypes in a database of tens of thousands of patients worldwide

If you are willing for information about you/your child to be entered in DECIPHER please complete and sign the DECIPHER research ethics consent form and return it to your geneticist.

DECIPHER helps the clinical community share and compare human genome variants and phenotypes in a database of tens of thousands of patients worldwide

This data is taken from open-access sequence variants in DECIPHER that have been assessed by the depositing centre as being pathogenic or likely pathogenic. Data from the CACNA1C …

DECIPHER has an advanced search facility that allows querying the database using a combination of terms including phenotypes, gene symbols, chromosomal locations/bands and …

The data is held in a linked anonymised form within the closed, password protected domain of an individual clinical genetics department that is affiliated to DECIPHER as a submitting centre.

The highlighted box on the gene name is a link out to the DECIPHER gene pages and provides collated information extracted from other patients that have openly accessible variants in this …

DECIPHER helps the clinical community share and compare human genome variants and phenotypes in a database of tens of thousands of patients worldwide