ClinVar Miner

Submissions for variant NM_004525.3(LRP2):c.7716-13dup

dbSNP: rs754348745
Minimum review status: Collection method:
Minimum conflict level:
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 RCV002129643 SCV002402939 benign not provided 2024-01-16 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500015 SCV002805268 likely benign Donnai-Barrow syndrome 2022-04-12 criteria provided, single submitter clinical testing

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