ClinVar Miner

Submissions for variant NM_001375808.2(LPIN2):c.2316C>A (p.Ser772=)

dbSNP: rs145270447
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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 RCV000644774 SCV000766487 likely benign Majeed syndrome 2017-12-14 criteria provided, single submitter clinical testing

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