ClinVar Miner

Submissions for variant NM_004525.3(LRP2):c.13519-40CT[7]

dbSNP: rs138614485
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002173632 SCV002429275 likely benign not provided 2023-12-08 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494328 SCV002795105 likely benign Donnai-Barrow syndrome 2021-10-08 criteria provided, single submitter clinical testing

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