ClinVar Miner

List of variants reported as uncertain significance 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.-4C>T	rs201541204	0.00053
NM_002857.4(PEX19):c.40G>C (p.Ala14Pro)	rs747627762	0.00005
NM_002857.4(PEX19):c.115C>T (p.Pro39Ser)	rs144256391

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