ClinVar Miner

Submissions for variant NM_003846.3(PEX11B):c.374+9T>C

gnomAD frequency: 0.00004  dbSNP: rs200094067
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000729167 SCV000856809 uncertain significance not provided 2017-09-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000729167 SCV001026859 benign not provided 2024-12-30 criteria provided, single submitter clinical testing

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