ClinVar Miner

Submissions for variant NM_004525.3(LRP2):c.246C>T (p.Pro82=)

dbSNP: rs1684836154
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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 RCV002108151 SCV002392928 likely benign not provided 2023-07-17 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002499983 SCV002809605 likely benign Donnai-Barrow syndrome 2022-03-22 criteria provided, single submitter clinical testing

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