"Institute of Human Genetics, University of Leipzig Medical Center"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 982776	NM_134261.3(RORA):c.1447C>T (p.Arg483Ter)	RORA, RORA-AS1 (R428* +3 more)	Single nucleotide variant (nonsense)	not provided +1 more	GUncertain significance
Select item 781175	NM_134261.3(RORA):c.196+51424G>A	RORA, RORA-AS1	Single nucleotide variant (intron variant)	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia +1 more	GBenign/Likely benign