ClinVar Miner

Submissions for variant NM_000411.8(HLCS):c.*40A>G (rs77014096)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000247568 SCV000304063 likely benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000394580 SCV000436038 likely benign Holocarboxylase synthetase deficiency 2016-06-14 criteria provided, single submitter clinical testing

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