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Genomic Variant Interpretation Course

March 31
University of Manchester, Oxford Road
Manchester, M13 9PL United Kingdom
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Genomic Variant Interpretation Course

The University of Manchester (UoM) have launched a new continuing professional development (CPD) course, funded by the HEE, which provides an introduction to the tools and procedures used in the interpretation of genetic variants in the clinical setting. This free course is aimed at Consultant Clinical geneticists, Genetic Counsellors (who have not undertaken STP training), …

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1:00 pm

Coronavirus and Familial Hypercholesterolaemia (FH) Dial-in

March 31 @ 1:00 pm - 2:00 pm
Online United Kingdom

An extra FH Intelligence Network teleconference will be held on Tuesday 31st March at 13:00 – 14:00, to discuss coronavirus and the impact on specialist services and people with FH.   Please dial in on 0800 368 0707 using participant pin: 7992828#   You are welcome to join the call and don't need an invitation …

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With any Whole Genome Sequencing (WGS) test ordered, a Record of Discussion (RoD) form will also need to be submitted. This document is to record the patient’s consent for genomic testing and their choice on taking part in research. Guidance on the patient choice conversation can be found here
 
This RoD form will be available for clinicians to download from this webpage. Once completed with the patient, it can be send to the lab with the corresponding test order form and sample.
Tests available to order will be listed in the National Genomic Test Directory. A test order form will soon be made available for clinicians on this webpage to download and complete. This form will include the address of the laboratory that the appropriate sample and completed form needs to be sent to.
 
Until the new Genomic Laboratory Service goes live, please continue to follow existing test order processes.
 
Later this year, the online test ordering tool for Whole Genome Sequencing will be integrated into the National Genomics Informatics System (NGIS) and clinicians will be able to search or filter to find a clinical indication, confirm eligibility criteria and start the test request process for their patient.