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		<title>Three NHS Genetics Labs Fail to Share Variant Data Vital for Rare Disease Diagnosis</title>
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		<pubDate>Thu, 08 Oct 2026 20:33:33 +0000</pubDate>
				<category><![CDATA[Health]]></category>
		<category><![CDATA[ClinVar]]></category>
		<category><![CDATA[data sharing]]></category>
		<category><![CDATA[Genetic Testing]]></category>
		<category><![CDATA[Genetic Variants]]></category>
		<category><![CDATA[Genomics]]></category>
		<category><![CDATA[Genomics Laboratory Hubs]]></category>
		<category><![CDATA[molecular diagnosis]]></category>
		<category><![CDATA[NHS]]></category>
		<category><![CDATA[patient advocacy]]></category>
		<category><![CDATA[rare diseases]]></category>
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		<category><![CDATA[variant interpretation]]></category>
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					<description><![CDATA[A BMJ investigation finds that three of England's seven NHS genetics laboratories are failing to routinely submit genetic variants to public databases such as ClinVar, delaying diagnosis and care for rare disease patients.]]></description>
		
		
		
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