ClinVar Miner

Submissions for variant NM_018451.5(CENPJ):c.*743_*746ACTT[5] (rs543069738)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000402029 SCV000383411 uncertain significance Seckel syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000313531 SCV000383412 uncertain significance Primary Microcephaly, Recessive 2016-06-14 criteria provided, single submitter clinical testing

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