List of variants in gene PEX26 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001127649.3(PEX26):c.325T>C (p.Tyr109His)	rs45567240	0.00190
NM_001127649.3(PEX26):c.200A>G (p.Asn67Ser)	rs201884779	0.00179
NM_001127649.3(PEX26):c.409G>C (p.Val137Leu)	rs142648687	0.00179
NM_001127649.3(PEX26):c.728C>T (p.Ala243Val)	rs149153003	0.00083
NM_001127649.3(PEX26):c.102C>G (p.Ala34=)

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