List of variants reported as uncertain significance for gray platelet syndrome by ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001377304.1(GFI1B):c.550C>T (p.Arg184Cys)	rs771408008	0.00006
NM_015175.3(NBEAL2):c.4361C>T (p.Thr1454Met)	rs371607035	0.00003
NM_001377304.1(GFI1B):c.551G>A (p.Arg184His)	rs570058270	0.00002
NM_015175.3(NBEAL2):c.6631G>A (p.Asp2211Asn)	rs781499875	0.00002
NM_001377304.1(GFI1B):c.581G>A (p.Cys194Tyr)	rs753406078	0.00001
NM_001377304.1(GFI1B):c.758G>A (p.Cys253Tyr)	rs1849225412
NM_001377304.1(GFI1B):c.981C>G (p.His327Gln)	rs147973999
NM_015175.3(NBEAL2):c.2044A>T (p.Ile682Phe)	rs773164015
NM_015175.3(NBEAL2):c.3907C>A (p.Pro1303Thr)
NM_015175.3(NBEAL2):c.4085G>A (p.Arg1362Gln)	rs781185845
NM_015175.3(NBEAL2):c.8164-1G>A	rs2107465570

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.