ClinVar Miner

Submissions for variant NM_001034852.3(SMOC1):c.126G>A (p.Gln42=)

dbSNP: rs3742909
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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 RCV000248068 SCV000306004 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001682996 SCV001898578 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001808684 SCV002057487 benign Microphthalmia with limb anomalies 2021-07-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001682996 SCV002353790 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001682996 SCV005291529 benign not provided criteria provided, single submitter not provided

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