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I want to report a variant that was found to be causal through the NGRL through ClinVar, can I?ΒΆ

Question

I want to report a variant that was found to be causal through the NGRL through ClinVar, can I?

Answer

No. This is best done through the NHS clinical and laboratory team and with access to the most complete information for assessing pathogenicity; this will also avoid unnecessary duplication.

Last updated

This page was last updated on the 08 Nov 2024.