List of variants reported as benign for Hyperthyroxinemia, familial dysalbuminemic

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: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000477.7(ALB):c.1668C>T (p.Leu556=)	rs962004	0.50892
NM_000477.7(ALB):c.615+14G>T	rs55861135	0.03126
NM_000477.7(ALB):c.271-8C>T	rs55888080	0.01379
NM_000477.7(ALB):c.616-3T>C	rs61375018	0.00846
NM_000477.7(ALB):c.843+10C>T	rs56379403	0.00821
NM_000477.7(ALB):c.1608T>C (p.Asp536=)	rs56042353	0.00602
NM_000477.7(ALB):c.*19C>T	rs61332165	0.00276
NM_000477.7(ALB):c.1290-6T>C	rs57705126	0.00234
NM_000477.7(ALB):c.1785+7C>T	rs141131597	0.00234
NM_000477.7(ALB):c.612A>G (p.Pro204=)	rs58639526	0.00205
NM_000477.7(ALB):c.891T>C (p.Ser297=)	rs56167251	0.00187
NM_000477.7(ALB):c.1230T>C (p.Asn410=)	rs35683929	0.00173
NM_000477.7(ALB):c.1191+11T>A	rs78977679	0.00025
NM_000477.7(ALB):c.248C>T (p.Ala83Val)	rs200736287

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.