ClinVar Miner

List of variants in gene F13A1 reported as likely benign for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
Download table as spreadsheet
HGVS dbSNP
NM_000129.3(F13A1):c.*112G>T rs3024463
NM_000129.3(F13A1):c.*126T>C rs1050782
NM_000129.3(F13A1):c.*160G>A rs1050783
NM_000129.3(F13A1):c.*221G>A rs3024464
NM_000129.3(F13A1):c.*743G>A rs12862
NM_000129.3(F13A1):c.*89A>G rs3024462
NM_000129.3(F13A1):c.*995G>T rs3024466
NM_000129.3(F13A1):c.-18-5dup rs750373197
NM_000129.3(F13A1):c.103G>T (p.Val35Leu) rs5985
NM_000129.3(F13A1):c.1694C>T (p.Pro565Leu) rs5982
NM_000129.3(F13A1):c.1704A>G (p.Glu568=) rs5986
NM_000129.3(F13A1):c.1951G>A (p.Val651Ile) rs5987
NM_000129.3(F13A1):c.1954G>C (p.Glu652Gln) rs5988
NM_000129.3(F13A1):c.996A>C (p.Pro332=) rs5981

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.