ClinVar Miner

Submissions for variant NM_004525.3(LRP2):c.1842G>A (p.Val614=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003015915 SCV003312595 likely benign not provided 2024-02-23 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005019558 SCV005652250 uncertain significance Donnai-Barrow syndrome 2024-04-18 criteria provided, single submitter clinical testing

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