"Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan"[submitte - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2628172	NM_005060.4(RORC):c.1396-68G>A	RORC	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2628210	NM_005060.4(RORC):c.1395+113T>G	RORC	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2688284	NM_005060.4(RORC):c.156+63CA[14]	RORC	Microsatellite (intron variant)	not specified	GBenign
Select item 2688334	NM_005060.4(RORC):c.156+81_156+82insCACACACT	RORC	Microsatellite (intron variant)	not specified	GBenign
Select item 2688285	NM_005060.4(RORC):c.156+79_156+80insCACACACG	RORC	Microsatellite (intron variant)	not specified	GBenign
Select item 2688254	NM_005060.4(RORC):c.156+73_156+74insCACACACT	RORC	Microsatellite (intron variant)	not specified	GBenign
Select item 2688335	NM_005060.4(RORC):c.156+71_156+72insCACACACT	RORC	Microsatellite (intron variant)	not specified	GBenign
Select item 2688208	NM_005060.4(RORC):c.156+62delinsACACACACA	RORC	Indel (intron variant)	not specified	GBenign
Select item 2688076	NM_005060.4(RORC):c.156+62G>A	RORC	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2687924	NM_005060.4(RORC):c.156+61_156+62insCACACACA	RORC	Microsatellite (intron variant)	not specified	GBenign
Select item 2688082	NM_005060.4(RORC):c.156+60G>A	RORC	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 1327967	NM_005060.4(RORC):c.156+24A>C	RORC	Single nucleotide variant (intron variant)	Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency +1 more	GBenign
Select item 2628168	NM_005060.4(RORC):c.70+3610C>T	RORC	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 1165101	NM_005060.4(RORC):c.41-17C>T	RORC	Single nucleotide variant (intron variant)	Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency +1 more	GBenign
Select item 2628195	NM_005060.4(RORC):c.40+752C>A	RORC	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2628199	NM_005060.4(RORC):c.40+537G>A	RORC	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2628121	NM_005060.4(RORC):c.40+437C>G	RORC	Single nucleotide variant (intron variant)	not specified	GBenign