ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.1582del (p.Leu528fs) (rs1060499647)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Institute of Human Genetics,Cologne University	RCV000461470	SCV000537308	pathogenic	Tuberous sclerosis 2		no assertion criteria provided	clinical testing

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