List of variants in gene combination LOC126806431, TTN reported by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 4

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.17312C>G (p.Thr5771Ser)	rs16866477	0.00593
NM_001267550.2(TTN):c.17048A>G (p.Tyr5683Cys)	rs72648942	0.00471
NM_001267550.2(TTN):c.17183-9T>C	rs141687561	0.00133
NM_001267550.2(TTN):c.17543G>A (p.Gly5848Glu)	rs185962498	0.00028

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.