List of variants in gene combination LOC130066940, PEX26 reported as uncertain significance for Zellweger spectrum disorders

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001127649.3(PEX26):c.23C>T (p.Ser8Phe)	rs749146718	0.00002
NM_001127649.3(PEX26):c.17C>T (p.Ser6Leu)	rs770013891
NM_001127649.3(PEX26):c.20C>T (p.Thr7Ile)	rs1273090730

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