ClinVar Miner

Submissions for variant NM_001122764.3(PPOX):c.1353T>C (p.Tyr451=)

gnomAD frequency: 0.00005  dbSNP: rs148292941
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 RCV003682337 SCV004406071 likely benign not provided 2023-05-28 criteria provided, single submitter clinical testing

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