What is DNA?
DNA can be thought of as a biological recipe book: its code helps cells make the proteins the body needs.
Genetic information can add useful context to a medical evaluation. The meaning of any result depends on personal history, family history and qualified clinical interpretation.
DNA, or deoxyribonucleic acid, is a long molecule containing genetic instructions. The human genome contains roughly 3.2 billion DNA bases.
DNA can be thought of as a biological recipe book: its code helps cells make the proteins the body needs.
Genetic testing analyzes DNA for variants that may be associated with inherited conditions or health risks. A result is one part of a broader clinical picture, not a diagnosis on its own.
Genome sequencingA screening conversation may consider both variants acquired over time and variants inherited through a family. Their importance varies by condition and by person.
Some DNA changes occur over time and may be influenced by cell division, aging or environmental exposures.
Some variants are present from birth and can be passed through one or both sides of a family.
The center offers Exome and proactive DNA testing using next-generation sequencing for panels described as covering more than 400 diseases and cancers. Panel coverage and eligibility should be confirmed before testing.

Linked conditions open the corresponding clinical guide. Inclusion here does not mean that screening alone confirms a diagnosis or determines treatment eligibility.
Contact the team to discuss the purpose of testing, panel availability and whether a pre-test counseling conversation is appropriate.
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