ClinVar Miner

Submissions for variant NM_004525.3(LRP2):c.13137C>G (p.Pro4379=)

dbSNP: rs140160600
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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 RCV002159953 SCV002412151 likely benign not provided 2023-11-07 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002508036 SCV002808490 likely benign Donnai-Barrow syndrome 2022-02-15 criteria provided, single submitter clinical testing

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