"Fulgent Genetics, Fulgent Genetics"[submitter] AND "TERC"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 39286	NR_001566.1(TERC):n.228G>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	not provided +3 more	GBenign/Likely benign
Select item 7323	NR_001566.1(TERC):n.58G>A	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	not specified +3 more	GBenign/Likely benign
Select item 39293	NR_001566.1(TERC):n.37A>G	TERC, LOC110806306	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1 +1 more	GUncertain significance
Select item 39292	NR_001566.1(TERC):n.35C>T	LOC110806306, TERC	Single nucleotide variant (non-coding transcript variant)	Dyskeratosis congenita, autosomal dominant 1 +1 more	GUncertain significance

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