"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC130009 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3055208	NM_001004127.3(ALG11):c.-9C>T	ALG11, LOC130009841	Single nucleotide variant (5 prime UTR variant +1 more)	ALG11-related disorder	GLikely benign
Select item 3048083	NM_001004127.3(ALG11):c.27C>T (p.Cys9=)	ALG11, LOC130009841	Single nucleotide variant (synonymous variant +1 more)	ALG11-related disorder	GLikely benign