List of variants reported as pathogenic for Telangiectasia, hereditary hemorrhagic, type 1 by OMIM

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: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001114753.3(ENG):c.1238G>T (p.Gly413Val)	rs121918401
NM_001114753.3(ENG):c.1553_1554del (p.Ser518fs)	rs2131875838
NM_001114753.3(ENG):c.2T>C (p.Met1Thr)	rs267606783
NM_001114753.3(ENG):c.360+1G>A	rs886039505
NM_001114753.3(ENG):c.360+4A>G	rs1564457752
NM_001114753.3(ENG):c.360C>A (p.Tyr120Ter)	rs121918402
NM_001114753.3(ENG):c.67+1G>A	rs1554813783
NM_001114753.3(ENG):c.831C>G (p.Tyr277Ter)	rs121918400
NM_001114753.3(ENG):c.882_920del (p.Thr295_Asn307del)	rs2131886961

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.