"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "TERC"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 570713	NR_001566.3(TERC):n.391C>T	TERC	Single nucleotide variant	not provided +1 more	GUncertain significance
Select item 1022075	NR_001566.3(TERC):n.246G>A	LOC110806306, TERC	Single nucleotide variant	not provided +1 more	GUncertain significance
Select item 1693878	NR_001566.3(TERC):n.172A>G	LOC110806306, TERC	Single nucleotide variant	not provided	GUncertain significance
Select item 1348970	NR_001566.3(TERC):n.66C>T	LOC110806306, TERC	Single nucleotide variant	not provided +1 more	GUncertain significance
Select item 2683780	NR_001566.3(TERC):n.61A>G	LOC110806306, TERC	Single nucleotide variant	not provided +1 more	GUncertain significance
Select item 30265	NR_001566.3(TERC):n.52_55delCTAA	LOC110806306, TERC	Deletion	Dyskeratosis congenita, autosomal dominant 1 +1 more	GPathogenic
Select item 1056990	NR_001566.3(TERC):n.35C>A	LOC110806306, TERC	Single nucleotide variant	Dyskeratosis congenita, autosomal dominant 1 +1 more	GUncertain significance

ClinVar