"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1285040	NM_001013838.3(CARMIL2):c.540C>T (p.Asp180=)	CARMIL2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1090061	NM_001013838.3(CARMIL2):c.810G>A (p.Ala270=)	CARMIL2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1164705	NM_001013838.3(CARMIL2):c.2286C>T (p.Ala762=)	CARMIL2	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign

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