ClinVar Miner

Submissions for variant NM_004525.3(LRP2):c.13218C>T (p.Thr4406=)

dbSNP: rs780040199
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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 RCV000977349 SCV001125265 likely benign not provided 2024-01-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002479146 SCV002804132 likely benign Donnai-Barrow syndrome 2022-03-13 criteria provided, single submitter clinical testing

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