ClinVar Miner

Submissions for variant NM_001034852.3(SMOC1):c.858-19C>A

gnomAD frequency: 0.15288  dbSNP: rs57609901
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243419 SCV000306006 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001682997 SCV001901296 benign not provided 2021-05-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001808686 SCV002057492 benign Microphthalmia with limb anomalies 2021-07-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001682997 SCV002332634 benign not provided 2025-02-02 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001682997 SCV005291540 benign not provided criteria provided, single submitter not provided

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