C4706604[trait identifier] AND "Daryl Scott Lab, Baylor College of Med - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1194018	NM_001286577.2(C2CD3):c.5882-332A>G	C2CD3	Single nucleotide variant (intron variant +1 more)	Orofaciodigital syndrome type 14 +1 more	GUncertain significance
Select item 599461	NM_001286577.2(C2CD3):c.704C>T (p.Pro235Leu)	C2CD3 (P235L)	Single nucleotide variant (missense variant)	Orofaciodigital syndrome type 14 +3 more	GBenign/Likely benign