ClinVar Miner

Submissions for variant NM_001375808.2(LPIN2):c.1422C>T (p.Cys474=)

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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 RCV003612232 SCV004537392 likely benign Majeed syndrome 2024-01-29 criteria provided, single submitter clinical testing

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