ClinVar Miner

List of variants reported as likely pathogenic for colonic neoplasm by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (19):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP
NM_000038.6(APC):c.1312+3A>G rs863225311
NM_000546.5(TP53):c.799C>T (p.Arg267Trp) rs55832599
NM_144997.7(FLCN):c.779+1G>T rs758175953

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.