"Genome-Nilou Lab"[submitter] AND "TBL1X"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1233016	NM_005647.4(TBL1X):c.749+15G>A	TBL1X	Single nucleotide variant (intron variant)	Hypothyroidism, congenital, nongoitrous, 8 +1 more	GBenign
Select item 1334929	NM_005647.4(TBL1X):c.749+22dup	TBL1X	Duplication (intron variant)	Hypothyroidism, congenital, nongoitrous, 8	GBenign
Select item 1334930	NM_005647.4(TBL1X):c.892-24G>T	TBL1X	Single nucleotide variant (intron variant)	Hypothyroidism, congenital, nongoitrous, 8 +1 more	GBenign
Select item 1334931	NM_005647.4(TBL1X):c.1054-41C>A	TBL1X	Single nucleotide variant (intron variant)	Hypothyroidism, congenital, nongoitrous, 8 +1 more	GBenign

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