Related gene-specific medical variations for Gene (Select 644990) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 901330	NM_001354712.2(THRB):c.-404T>C	THRB, THRB-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	Thyroid hormone resistance, generalized, autosomal dominant	GUncertain significance
Select item 901329	NM_001354712.2(THRB):c.-367G>A	THRB, THRB-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	Thyroid hormone resistance, generalized, autosomal dominant	GUncertain significance
Select item 901328	NM_001354712.2(THRB):c.-274G>T	THRB, THRB-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	Thyroid hormone resistance, generalized, autosomal dominant	GUncertain significance
Select item 344645	NM_001354712.2(THRB):c.-393T>C	THRB-AS1, THRB	Single nucleotide variant (5 prime UTR variant +1 more)	Thyroid hormone resistance, generalized, autosomal dominant	GUncertain significance
Select item 344644	NM_001354712.2(THRB):c.-385GA[1]	THRB, THRB-AS1	Microsatellite (5 prime UTR variant +1 more)	Thyroid hormone resistance syndrome	GUncertain significance
Select item 344643	NM_001354712.2(THRB):c.-261+5G>C	THRB, THRB-AS1	Single nucleotide variant (intron variant)	Thyroid hormone resistance, generalized, autosomal dominant	GUncertain significance

ClinVar