The main purpose of this Manual is to provide useful guidelines for the selection of pathology tests and to facilitate interpretation of results.
Contains a comprehensive listing of all genes from the Human Gene Nomenclature Committee (HGNC) database alongside laboratories and tests available in the country.
A manual for the process of macroscopic dissection in Anatomical Pathology laboratories.
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SCN5A (also called Nav1.5,LQT3,HB1,HBBD,PFHB1,IVF,HB2,HH1,SSS1,CDCD2,CMPD2,ICCD)
sodium voltage-gated channel alpha subunit 5 (OMIM 600163)
OMIM 601154 : Cardiomyopathy, dilated, 1E OMIM 113900 : Heart block, nonprogressive OMIM 113900 : Heart block, progressive, type IA OMIM 614022 : Atrial fibrillation, familial, 10 OMIM 272120 : Sudden infant death syndrome, susceptibility to OMIM 608567 : Sick sinus syndrome 1 OMIM 603829 : Ventricular fibrillation, familial, 1 OMIM 603830 : Long QT syndrome 3 OMIM 601144 : Brugada syndrome 1
Laboratory methods do not necessarily identify all of the clinically significant variants in a gene. The failure to identify a variant does not necessarily mean that the gene is normal. Variants in a gene may cause more than one disease, and the identification of a clinically significant variant does not necessarily indicate the specific disease that the patient or relatives may be at risk of developing. Conversely, the disease/s associated with a gene might also be caused by mutations in other genes, and the failure to identify a clinically significant variant in one gene does not necessarily alter the clinical diagnosis or risk for relatives.
20/01/2023
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The RCPA is the leading organisation representing Pathologists and Senior Scientists in Australasia.
Its mission is to train and support pathologists and senior scientists and to improve the use of pathology testing to achieve better healthcare.
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