ClinVar Miner

List of variants in gene F7 reported as likely benign for congenital vitamin K-dependent coagulation factors deficiency

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP
NM_000131.4(F7):c.108G>A (p.Pro36=) rs3093238
NM_000131.4(F7):c.64+4C>T rs187128791
NM_000131.4(F7):c.64+8C>T rs10482844
NM_019616.4(F7):c.*1503C>T
NM_019616.4(F7):c.1104C>T (p.Ala368=) rs6044
NM_019616.4(F7):c.1292C>T (p.Ser431Leu)
NM_019616.4(F7):c.84A>C (p.Glu28Asp)

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.