ClinVar Miner

Submissions for variant NM_207352.4(CYP4V2):c.1329G>A (p.Arg443=)

gnomAD frequency: 0.00067  dbSNP: rs150506310
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001522806 SCV001732418 benign not provided 2024-11-25 criteria provided, single submitter clinical testing

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