ClinVar Miner

Submissions for variant NM_133433.4(NIPBL):c.-428G>C (rs886060551)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Illumina Clinical Services Laboratory,Illumina	RCV000307141	SCV000457250	uncertain significance	Cornelia de Lange Syndrome	2016-06-14	criteria provided, single submitter	clinical testing

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