ClinVar Miner

Submissions for variant NM_004525.3(LRP2):c.573C>T (p.Gly191=)

dbSNP: rs1254126085
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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 RCV002048267 SCV002303665 likely benign not provided 2023-10-18 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002479789 SCV002777436 uncertain significance Donnai-Barrow syndrome 2021-12-22 criteria provided, single submitter clinical testing

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