ClinVar for MedGen (Select 448009) - ClinVar

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Result Filters

VariationLocation		Gene(s)	Protein change	Condition(s)	Clinical significance (Last reviewed)	Review status
Select item 3682791.	NM_001378477.3(NYX):c.734_735dup GRCh37: ChrX:41334874-41334875 GRCh38: ChrX:41475621-41475622	NYX		X-linked congenital stationary night blindness	Uncertain significance (Jun 14, 2016)	criteria provided, single submitter
Select item 3682732.	NM_001378477.3(NYX):c.*16del GRCh37: ChrX:41334163 GRCh38: ChrX:41474910	NYX		X-linked congenital stationary night blindness	Uncertain significance (Jun 14, 2016)	criteria provided, single submitter