ClinVar Miner

Submissions for variant NM_004525.3(LRP2):c.13519-40CT[8]

dbSNP: rs138614485
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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 RCV002136207 SCV002462197 likely benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002486966 SCV002795574 likely benign Donnai-Barrow syndrome 2021-12-02 criteria provided, single submitter clinical testing

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