ClinVar Miner

List of variants reported as likely benign for brain-lung-thyroid syndrome

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP
NM_001079668.3(NKX2-1):c.*14C>T rs755542970
NM_001079668.3(NKX2-1):c.*209T>A rs572546897
NM_001079668.3(NKX2-1):c.*436A>C rs79849967
NM_001079668.3(NKX2-1):c.*579C>G rs566916288
NM_001079668.3(NKX2-1):c.*581del rs534281105
NM_001079668.3(NKX2-1):c.1093G>T (p.Ala365Ser) rs147542347
NM_001079668.3(NKX2-1):c.1106C>T (p.Ala369Val) rs537209983
NM_001079668.3(NKX2-1):c.29G>A (p.Arg10Gln) rs201979429
NM_001079668.3(NKX2-1):c.535G>T (p.Val179Leu) rs575848748

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.