ClinVar Miner

List of variants in gene F11 reported as likely pathogenic by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
Download table as spreadsheet
HGVS dbSNP
NC_000004.12:g.(?_186287674)_(186287834_?)dup
NM_000128.3(F11):c.486-2A>G rs1057516695
NM_000128.4(F11):c.595+3A>G rs933333847
NM_000128.4(F11):c.865+1G>A

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.