ClinVar Miner

Submissions for variant NM_004525.3(LRP2):c.10572-13G>A

gnomAD frequency: 0.00004  dbSNP: rs372963344
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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 RCV002138272 SCV002458024 likely benign not provided 2024-01-12 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494441 SCV002804914 likely benign Donnai-Barrow syndrome 2022-05-18 criteria provided, single submitter clinical testing

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