List of variants in gene LTBP3 reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001130144.3(LTBP3):c.132del (p.Pro45fs)	rs1286042594
NM_001130144.3(LTBP3):c.1531+1G>T	rs875989823
NM_001130144.3(LTBP3):c.1846+5G>A	rs1188540819
NM_001130144.3(LTBP3):c.1859dup (p.Cys620fs)	rs878853262
NM_001130144.3(LTBP3):c.2071_2084del (p.Tyr691fs)	rs875989822
NM_001130144.3(LTBP3):c.2087C>G (p.Ser696Cys)	rs1554974135
NM_001130144.3(LTBP3):c.2356del (p.Val786fs)	rs875989824
NM_001130144.3(LTBP3):c.3912A>T (p.Ter1304Cys)	rs1554971742
NM_001130144.3(LTBP3):c.421C>T (p.Gln141Ter)	rs796052116

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.