"PreventionGenetics, part of Exact Sciences"[submitter] AND "FOXC2-AS1 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 259691	NM_005251.3(FOXC2):c.108C>T (p.Ser36=)	FOXC2, FOXC2-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2631715	NM_005251.3(FOXC2):c.251C>A (p.Ala84Asp)	FOXC2, FOXC2-AS1 (A84D)	Single nucleotide variant (missense variant)	FOXC2-related condition	GUncertain significance
Select item 3056999	NM_005251.3(FOXC2):c.312C>T (p.Asp104=)	FOXC2, FOXC2-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	FOXC2-related condition	GLikely benign
Select item 259694	NM_005251.3(FOXC2):c.351G>A (p.Gln117=)	FOXC2-AS1, FOXC2	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3061401	NM_005251.3(FOXC2):c.365A>C (p.His122Pro)	FOXC2, FOXC2-AS1 (H122P)	Single nucleotide variant (non-coding transcript variant +1 more)	FOXC2-related condition	GUncertain significance
Select item 259695	NM_005251.3(FOXC2):c.411C>T (p.Asp137=)	FOXC2, FOXC2-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign

ClinVar