ClinVar Miner

List of variants reported as benign for Factor v and factor viii, combined deficiency of, 2

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 25
Download table as spreadsheet
HGVS dbSNP
NM_001171506.2(MCFD2):c.*1010G>T rs138758588
NM_001171506.2(MCFD2):c.*1042C>T rs111603188
NM_001171506.2(MCFD2):c.*1043G>A rs114662283
NM_001171506.2(MCFD2):c.*1267G>T rs7596245
NM_001171506.2(MCFD2):c.*133A>T rs75416242
NM_001171506.2(MCFD2):c.*1346G>T rs111535939
NM_001171506.2(MCFD2):c.*1525C>G rs7596198
NM_001171506.2(MCFD2):c.*1677T>G rs28770495
NM_001171506.2(MCFD2):c.*1724C>T rs115137793
NM_001171506.2(MCFD2):c.*1752T>C rs6544935
NM_001171506.2(MCFD2):c.*1788C>T rs115043642
NM_001171506.2(MCFD2):c.*1908G>C rs6743994
NM_001171506.2(MCFD2):c.*1924T>C rs6715391
NM_001171506.2(MCFD2):c.*2075C>T rs6743966
NM_001171506.2(MCFD2):c.*2163A>G rs140937815
NM_001171506.2(MCFD2):c.*2336A>C rs144118640
NM_001171506.2(MCFD2):c.*2454C>A rs1051317
NM_001171506.2(MCFD2):c.*2658C>T rs17035887
NM_001171506.2(MCFD2):c.*2675C>G rs17035884
NM_001171506.2(MCFD2):c.*3100C>G rs13424086
NM_001171506.2(MCFD2):c.*3318T>C rs8861
NM_001171506.2(MCFD2):c.*498A>G rs144674773
NM_001171506.2(MCFD2):c.*693G>C rs28516550
NM_001171506.2(MCFD2):c.*73A>G rs71423925
NM_139279.6(MCFD2):c.*1124G>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.