"Fulgent Genetics, Fulgent Genetics"[submitter] AND "RORC"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1028332	NM_005060.4(RORC):c.1535C>G (p.Ser512Ter)	RORC (S512* +1 more)	Single nucleotide variant (nonsense)	Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency	GUncertain significance
Select item 475712	NM_005060.4(RORC):c.28C>T (p.Arg10Ter)	RORC (R10*)	Single nucleotide variant (nonsense)	Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency	GLikely benign

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