ClinVar Miner

Submissions for variant NM_001039213.4(CEACAM16):c.383-5C>A

gnomAD frequency: 0.00010  dbSNP: rs201855875
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
GeneDx RCV000827294 SCV000968931 likely benign not provided 2021-03-31 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000827294 SCV002936203 benign not provided 2024-10-13 criteria provided, single submitter clinical testing

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