C4014745[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 520872	NM_001080510.5(METTL23):c.20C>T (p.Ala7Val)	METTL23 (A7V)	Single nucleotide variant (missense variant +2 more)	not provided +2 more	GUncertain significance
Select item 1031798	NM_001080510.5(METTL23):c.250A>G (p.Ile84Val)	METTL23 (I80V +2 more)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal recessive 44	GUncertain significance
Select item 1712311	NM_001080510.5(METTL23):c.266T>A (p.Leu89Gln)	METTL23 (L22Q +2 more)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal recessive 44	GUncertain significance
Select item 1032598	NM_001080510.5(METTL23):c.319G>A (p.Glu107Lys)	METTL23 (E103K +2 more)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal recessive 44	GUncertain significance
Select item 1032599	NM_001080510.5(METTL23):c.417G>T (p.Trp139Cys)	METTL23 (W135C +2 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability, autosomal recessive 44	GUncertain significance
Select item 1032600	NM_001080510.5(METTL23):c.496G>T (p.Asp166Tyr)	METTL23 (D166Y +2 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability, autosomal recessive 44	GUncertain significance
Select item 1031045	NM_001080510.5(METTL23):c.521G>T (p.Gly174Val)	METTL23 (G107V +2 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability, autosomal recessive 44	GUncertain significance

ClinVar