List of variants in gene combination LOC110806306, TERC reported as uncertain significance for hematologic disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NR_001566.3(TERC):n.37A>G	rs199422261	0.00003
NR_001566.3(TERC):n.35C>T	rs199422260	0.00001
NR_001566.3(TERC):n.36C>T	rs1248582778	0.00001

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