ClinVar Miner

Submissions for variant NM_000466.3(PEX1):c.3637-6C>T

dbSNP: rs2116039914
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001481630 SCV001685978 likely benign Zellweger spectrum disorders 2019-12-06 criteria provided, single submitter clinical testing

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