"ALG10-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3057080	NM_032834.4(ALG10):c.354A>G (p.Val118=)	ALG10	Single nucleotide variant (synonymous variant)	ALG10-related disorder	GLikely benign
Select item 785400	NM_032834.4(ALG10):c.402A>C (p.Thr134=)	ALG10	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3040080	NM_032834.4(ALG10):c.1366C>T (p.Leu456=)	ALG10	Single nucleotide variant (synonymous variant)	ALG10-related disorder	GLikely benign

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