ClinVar Miner

List of variants reported as not provided by TNNI2 homepage - Leiden Muscular Dystrophy pages

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP
NM_003282.4(TNNI2):c.15+140C>A rs1877444
NM_003282.4(TNNI2):c.15+21C>G rs2292476
NM_003282.4(TNNI2):c.186+26G>A rs2271441
NM_003282.4(TNNI2):c.466C>T (p.Arg156Ter) rs104894312
NM_003282.4(TNNI2):c.496_498GAG[1] (p.Glu167del) rs199474800
NM_003282.4(TNNI2):c.521G>A (p.Arg174Gln) rs104894311
NM_003282.4(TNNI2):c.524_526AGA[1] (p.Lys176del) rs199474801
NM_003282.4(TNNI2):c.60T>C (p.Ser20=) rs907610

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.