ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.16273A>G (p.Asn5425Asp)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003872892 SCV004672553 benign not provided 2023-11-14 criteria provided, single submitter clinical testing
GeneDx RCV003872892 SCV005333714 uncertain significance not provided 2023-08-21 criteria provided, single submitter clinical testing In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge

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