DECIPHER is used by the clinical community to share and compare phenotypic and genotypic data. The DECIPHER database contains data from 51,825 patients who have given consent …

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

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 maintains a regularly updated list of known genes from HGNC with location information derived from Ensembl and UCSC. In addition DECIPHER also maintains a list of …

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

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

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

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