ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.684T>C (p.Asn228=)

gnomAD frequency: 0.00051  dbSNP: rs181889432
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000353953 SCV000341082 uncertain significance not provided 2016-05-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000353953 SCV001694652 likely benign not provided 2024-12-19 criteria provided, single submitter clinical testing
GeneDx RCV000353953 SCV001805024 likely benign not provided 2020-11-20 criteria provided, single submitter clinical testing

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