ClinVar Miner

Submissions for variant NM_002857.4(PEX19):c.25A>G (p.Ser9Gly)

dbSNP: rs775660692
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001335072 SCV001528114 uncertain significance Peroxisome biogenesis disorder 12A (Zellweger) 2018-01-13 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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