ClinVar Miner

Submissions for variant NM_004525.3(LRP2):c.2909-19C>T

gnomAD frequency: 0.00087  dbSNP: rs144286272
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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 RCV002073812 SCV002376167 benign not provided 2024-01-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507932 SCV002795679 likely benign Donnai-Barrow syndrome 2022-02-03 criteria provided, single submitter clinical testing

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