ClinVar Miner

Submissions for variant NM_207352.4(CYP4V2):c.1362A>G (p.Pro454=)

gnomAD frequency: 0.00001  dbSNP: rs1038955378
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001303440 SCV001492686 likely benign not provided 2022-10-17 criteria provided, single submitter clinical testing

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