ClinVar Miner

List of variants reported as likely benign for Peroxisome biogenesis disorder 12A (Zellweger) by Fulgent Genetics, Fulgent Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002857.4(PEX19):c.879T>C (p.Gly293=)	rs74125561	0.01345
NM_002857.4(PEX19):c.346+14A>G	rs77156017	0.00182
NM_002857.4(PEX19):c.181-15A>G	rs114403769

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