ClinVar Miner

Submissions for variant NM_207352.4(CYP4V2):c.1114G>A (p.Val372Ile)

gnomAD frequency: 0.00633  dbSNP: rs61755911
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
Invitae RCV000087016 SCV001027791 benign not provided 2024-01-24 criteria provided, single submitter clinical testing
NEI Ophthalmic Genomics Laboratory, National Institutes of Health RCV000087016 SCV000119269 not provided not provided no assertion provided not provided

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