ClinVar Miner

Submissions for variant NM_016952.4(CDON):c.*2640A>G (rs886047951)

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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	RCV000388665	SCV000368623	uncertain significance	Holoprosencephaly sequence	2016-06-14	criteria provided, single submitter	clinical testing

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