ClinVar Miner

List of variants in gene F2 reported as 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: 11
Download table as spreadsheet
HGVS dbSNP
NM_000506.4(F2):c.1233G>A (p.Pro411=) rs5898
NM_000506.4(F2):c.1602G>A (p.Pro534=) rs5900
NM_000506.4(F2):c.1628G>T (p.Arg543Leu) rs143064939
NM_000506.4(F2):c.423-7G>C rs2070852
NM_000506.4(F2):c.480C>T (p.Pro160=) rs3136452
NM_000506.4(F2):c.494C>T (p.Thr165Met) rs5896
NM_000506.4(F2):c.79+7G>A rs3136431
NM_000506.4(F2):c.813C>T (p.Gly271=) rs5899
NM_000506.5(F2):c.*97G>A rs1799963
NM_000506.5(F2):c.1857G>A (p.Gln619=) rs113406770
NM_000506.5(F2):c.843C>T (p.Gly281=) rs147699032

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.