ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.1189A>G (p.Ser397Gly)

gnomAD frequency: 0.00002  dbSNP: rs377201437
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000733422 SCV000861490 uncertain significance not provided 2018-06-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000733422 SCV004629554 benign not provided 2024-03-07 criteria provided, single submitter clinical testing

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