ClinVar for MedGen (Select 448009) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 368279	NM_001378477.3(NYX):c.734_735dup	NYX	Duplication (3 prime UTR variant)	X-linked congenital stationary night blindness	GUncertain significance
Select item 368273	NM_001378477.3(NYX):c.*16del	NYX	Deletion (3 prime UTR variant)	X-linked congenital stationary night blindness +1 more	GUncertain significance