"PreventionGenetics, part of Exact Sciences"[submitter] AND "CYB561"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3051792	NM_001915.4(CYB561):c.606C>T (p.Asn202=)	CYB561	Single nucleotide variant (synonymous variant)	CYB561-related disorder	GLikely benign
Select item 3046415	NM_001915.4(CYB561):c.561C>T (p.Leu187=)	CYB561	Single nucleotide variant (synonymous variant)	CYB561-related disorder	GLikely benign
Select item 3040835	NM_001915.4(CYB561):c.318C>T (p.Phe106=)	CYB561	Single nucleotide variant (synonymous variant)	CYB561-related disorder	GLikely benign
Select item 3034465	NM_001915.4(CYB561):c.207G>A (p.Leu69=)	CYB561	Single nucleotide variant (synonymous variant)	CYB561-related disorder	GBenign
Select item 3060907	NM_001915.4(CYB561):c.24C>T (p.Ala8=)	CYB561	Single nucleotide variant (synonymous variant)	CYB561-related disorder	GLikely benign
Select item 3056754	NM_001915.4(CYB561):c.-13-2648G>A	CYB561	Single nucleotide variant (5 prime UTR variant +1 more)	CYB561-related disorder	GBenign

ClinVar