ClinVar Miner

List of variants in gene combination LOC110806306, TERC reported as uncertain significance for anemia (disease)

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP
NR_001566.1(TERC):n.11G>T rs1159032173
NR_001566.1(TERC):n.20T>C rs1060502987
NR_001566.1(TERC):n.29T>A rs1336050074
NR_001566.1(TERC):n.36C>T rs1248582778
NR_001566.1(TERC):n.37A>G rs199422261
NR_001566.1(TERC):n.42_43dup
NR_001566.1(TERC):n.43T>G rs1553915624
NR_001566.1(TERC):n.7C>A rs781517281

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.