ClinVar Miner

Submissions for variant NM_004991.4(MECOM):c.2771+4A>G

gnomAD frequency: 0.00003  dbSNP: rs773749114
Minimum review status: Collection method:
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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
Genetic Services Laboratory, University of Chicago RCV001822789 SCV002070408 likely benign not specified 2021-12-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003708618 SCV004472860 likely benign not provided 2024-07-23 criteria provided, single submitter clinical testing

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