C4310633[trait identifier] AND "Victorian Clinical Genetics Services, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1806094	NM_014727.3(KMT2B):c.1102A>C (p.Lys368Gln)	KMT2B (K368Q)	Single nucleotide variant (missense variant)	Dystonia 28, childhood-onset	GUncertain significance
Select item 1806273	NM_014727.3(KMT2B):c.3370C>T (p.Pro1124Ser)	KMT2B (P1124S)	Single nucleotide variant (missense variant)	Dystonia 28, childhood-onset	GUncertain significance