List of variants in gene PEX10 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002617.4(PEX10):c.6C>G (p.Ala2=)	rs112471479	0.00523
NM_002617.4(PEX10):c.627G>A (p.Glu209=)	rs141430704	0.00043
NM_002617.4(PEX10):c.771C>T (p.His257=)	rs776503441	0.00006
NM_002617.4(PEX10):c.897G>A (p.Ala299=)	rs372779905	0.00001

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