DECIPHER v11.34: Mapping the clinical genome
DECIPHER is used by the clinical community to share and compare phenotypic and genotypic data. The DECIPHER database contains data from 51,551 patients who have given consent …
Genes with Sequence Variants - DECIPHER v11.34
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 …
Deciphering Developmental Disorders - DECIPHER v11.34
DECIPHER helps the clinical community share and compare human genome variants and phenotypes in a database of tens of thousands of patients worldwide
CACNA1A - DECIPHER v11.34
DECIPHER helps the clinical community share and compare human genome variants and phenotypes in a database of tens of thousands of patients worldwide
EP300 - DECIPHER v11.34
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 …
TLK2 - DECIPHER v11.34
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 TLK2 gene is …
SMC1A - DECIPHER v11.34
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.
API Documentation - DECIPHER v11.34
The DECIPHER deposition API is designed to allow users of DECIPHER to deposit patient data to DECIPHER from third-party clients. Patient data includes basic unidentifiable information, …