ClinVar Miner

Submissions for variant NM_003846.3(PEX11B):c.291C>T (p.Phe97=)

gnomAD frequency: 0.00003  dbSNP: rs151338360
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 RCV001518043 SCV001726673 benign not provided 2024-03-24 criteria provided, single submitter clinical testing

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