ClinVar Miner

Submissions for variant NM_003906.5(MCM3AP):c.3684_3695del (p.Ala1229_Thr1232del)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003132612 SCV003810830 uncertain significance Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development 2022-05-24 criteria provided, single submitter clinical testing

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