ClinVar Miner

List of variants reported as likely pathogenic for Familial hemolytic anemia by Department of Genetic, Henri Mondor Hospital, Assistance Publique des Hôpitaux de Paris

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: 3

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_003126.4(SPTA1):c.6672A>C (p.Glu2224Asp)	rs142775522	0.00499
NM_001360016.2(G6PD):c.448G>A (p.Val150Ile)	rs1557230573
NM_003126.4(SPTA1):c.6600+5G>T	rs1462060431

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.