ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.1210G>A (p.Val404Ile)

gnomAD frequency: 0.00002  dbSNP: rs780748586
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000731063 SCV000858834 uncertain significance not provided 2018-01-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000731063 SCV001537805 benign not provided 2023-10-22 criteria provided, single submitter clinical testing

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