ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.3819G>A (p.Arg1273=)

gnomAD frequency: 0.00004  dbSNP: rs764738838
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) RCV000288423 SCV000345420 uncertain significance not provided 2016-09-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000288423 SCV001682659 likely benign not provided 2024-03-11 criteria provided, single submitter clinical testing

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