"METTL23-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 376858	NM_001080510.5(METTL23):c.136G>C (p.Glu46Gln)	METTL23 (E46Q +1 more)	Single nucleotide variant (missense variant +1 more)	METTL23-related disorder +1 more	GBenign/Likely benign
Select item 3060532	NM_001080510.5(METTL23):c.366G>C (p.Lys122Asn)	METTL23 (K118N +2 more)	Single nucleotide variant (missense variant +1 more)	METTL23-related disorder	GLikely benign