ClinVar Miner

Submissions for variant NM_001375808.2(LPIN2):c.1169-7dup

dbSNP: rs746626720
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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 RCV002122932 SCV002410552 benign Majeed syndrome 2025-01-29 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV002122932 SCV004563990 likely benign Majeed syndrome 2024-03-28 criteria provided, single submitter clinical testing

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