" /> dbSNP:ID:Pt: Patient:Nom: - CISMeF





Preferred Label : dbSNP:ID:Pt: Patient:Nom:;

LOINC status : TRIAL;

LOINC display name : dbSNP Nom [ID];

LOINC long common name : dbSNP [ID];

LOINC short name : dbSNP ID;

LOINC description : The unique identifier for the variant represented as a small nucleotide polymorphism (SNP). The dbSNP ID is used routinely as the base identifier in pharmacogenomics as well as arrCGH studies. For example, for the simple variant NM_014049.4(ACAD9):c.1249C T (p.Arg417Cys), the dbSNP ID is 368949613. [http://www.ncbi.nlm.nih.gov/clinvar/variation/30880/];

Details


You can consult :


Nous contacter.
01/05/2025


[Home] [Top]

© Rouen University Hospital. Any partial or total use of this material must mention the source.