ClinVar Miner

Submissions for variant NM_022458.4(LMBR1):c.424-218dup

dbSNP: rs200856353
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
GeneDx RCV001538528 SCV001756193 likely benign not provided 2019-09-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002071939 SCV002419157 benign Holoprosencephaly 3 2025-02-03 criteria provided, single submitter clinical testing

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