"PreventionGenetics, part of Exact Sciences"[submitter] AND "CYP26C1"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 717978	NM_183374.3(CYP26C1):c.184A>T (p.Thr62Ser)	CYP26C1 (T62S)	Single nucleotide variant (missense variant)	CYP26C1-related disorder +1 more	GBenign/Likely benign
Select item 3058564	NM_183374.3(CYP26C1):c.459G>T (p.Ala153=)	CYP26C1, LOC130004370	Single nucleotide variant (synonymous variant)	CYP26C1-related disorder	GLikely benign
Select item 3039433	NM_183374.3(CYP26C1):c.522G>C (p.Ala174=)	CYP26C1, LOC130004371	Single nucleotide variant (synonymous variant)	CYP26C1-related disorder	GLikely benign
Select item 773001	NM_183374.3(CYP26C1):c.713G>A (p.Arg238Gln)	CYP26C1 (R238Q)	Single nucleotide variant (missense variant)	CYP26C1-related disorder +1 more	GBenign
Select item 784516	NM_183374.3(CYP26C1):c.1401C>G (p.Ala467=)	CYP26C1	Single nucleotide variant (synonymous variant)	CYP26C1-related disorder +1 more	GBenign/Likely benign
Select item 3034234	NM_183374.3(CYP26C1):c.1491C>T (p.Ile497=)	CYP26C1	Single nucleotide variant (synonymous variant)	CYP26C1-related disorder	GLikely benign

ClinVar