List of variants reported as benign for Factor XIII, A subunit, deficiency of by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000129.4(F13A1):c.-19+12A>C	rs2815822	0.88252
NM_000129.4(F13A1):c.*126T>C	rs1050782	0.52358
NM_000129.4(F13A1):c.103G>T (p.Val35Leu)	rs5985	0.22002
NM_000129.4(F13A1):c.1954G>C (p.Glu652Gln)	rs5988	0.21467
NM_000129.4(F13A1):c.1694C>T (p.Pro565Leu)	rs5982	0.18893
NM_000129.4(F13A1):c.*160G>A	rs1050783	0.18575
NM_000129.4(F13A1):c.996A>C (p.Pro332=)	rs5981	0.15230
NM_000129.4(F13A1):c.*995G>T	rs3024466	0.13914
NM_000129.4(F13A1):c.1951G>A (p.Val651Ile)	rs5987	0.05207
NM_000129.4(F13A1):c.*89A>G	rs3024462	0.04627
NM_000129.4(F13A1):c.*743G>A	rs12862	0.04625
NM_000129.4(F13A1):c.*221G>A	rs3024464	0.04624

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.