ClinVar Miner

Submissions for variant NM_004525.3(LRP2):c.80-10A>G

gnomAD frequency: 0.00001  dbSNP: rs769089398
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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 RCV002083197 SCV002371508 likely benign not provided 2023-10-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002498277 SCV002813132 likely benign Donnai-Barrow syndrome 2022-05-07 criteria provided, single submitter clinical testing

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