"Illumina Laboratory Services, Illumina"[submitter] AND "LOC130000261" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 909350	NM_003816.3(ADAM9):c.-18C>G	ADAM9, LOC130000261	Single nucleotide variant (non-coding transcript variant +1 more)	Cone-rod dystrophy 9	GUncertain significance
Select item 259176	NM_003816.3(ADAM9):c.78C>A (p.Val26=)	ADAM9, LOC130000261	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign