ClinVar Miner

Submissions for variant NM_016952.4(CDON):c.*2373_*2378del (rs886047957)

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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 RCV000313468 SCV000368639 uncertain significance Holoprosencephaly sequence 2016-06-14 criteria provided, single submitter clinical testing

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