ClinVar Miner

Submissions for variant NM_001375808.2(LPIN2):c.699-13_699-12dup

dbSNP: rs775605400
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001697962 SCV000723667 likely benign not provided 2020-03-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001514841 SCV001722784 benign Majeed syndrome 2024-01-29 criteria provided, single submitter clinical testing

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