ClinVar Miner

Submissions for variant NM_004817.4(TJP2):c.1520+6T>C (rs886044597)

Minimum review status:		Collection method:
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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics	RCV000318654	SCV000345624	uncertain significance	not provided	2016-08-25	criteria provided, single submitter	clinical testing

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