Variants in gene TNNI3 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.373-4C>G	rs2288530	0.00007
NM_000363.5(TNNI3):c.139T>C (p.Leu47=)	rs587780967	0.00006
NM_000363.5(TNNI3):c.372+7C>T	rs367809676	0.00004
NM_000363.5(TNNI3):c.-8G>A	rs773513015	0.00003
NM_000363.5(TNNI3):c.304G>A (p.Ala102Thr)	rs374618872	0.00003
NM_000363.5(TNNI3):c.151-6C>G	rs377258542	0.00002
NM_000363.5(TNNI3):c.340A>G (p.Ile114Val)	rs730881070	0.00001
NM_000363.5(TNNI3):c.34C>T (p.Pro12Ser)	rs553214254	0.00001
NM_000363.5(TNNI3):c.12-7del	rs370714315
NM_000363.5(TNNI3):c.157C>T (p.Leu53=)	rs763981651

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.