List of variants in gene PEX6 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000287.4(PEX6):c.853C>G (p.Pro285Ala)	rs61753220	0.00067
NM_000287.4(PEX6):c.970G>A (p.Glu324Lys)	rs201678533	0.00010
NM_000287.4(PEX6):c.939T>C (p.Pro313=)	rs151234121	0.00004
NM_000287.4(PEX6):c.348C>T (p.Leu116=)	rs746578841	0.00001
NM_000287.4(PEX6):c.1479+7G>A	rs528161793
NM_000287.4(PEX6):c.303G>A (p.Pro101=)	rs1032414476
NM_000287.4(PEX6):c.831G>A (p.Leu277=)

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