List of variants in gene TERC reported as pathogenic for anemia

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
NC_000003.12:g.169764611C>T	rs199422287	0.00001
NR_001566.1(TERC):n.407_408delinsAA	rs1553915580
NR_001566.3(TERC):n.389_390delCC	rs199422283

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