ClinVar Genomic variation as it relates to human health
NM_001276345.2(TNNT2):c.412-6_412-4del
Germline
Classification
(9)
Benign/Likely benign
criteria provided, multiple submitters, no conflicts
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
TNNT2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
956 | 975 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign/Likely benign (2) |
|
Jun 12, 2023 | RCV000036582.6 | |
Benign (2) |
|
Oct 21, 2020 | RCV000771864.4 | |
Benign (1) |
|
Apr 11, 2023 | RCV003445103.1 | |
Likely benign (1) |
|
Jan 22, 2020 | RCV004018796.1 | |
Likely benign (1) |
|
Jan 28, 2024 | RCV000560677.9 | |
Benign (1) |
|
Apr 11, 2023 | RCV003445104.1 | |
Benign (1) |
|
Apr 11, 2023 | RCV003445105.1 |
Citations for germline classification of this variant
HelpText-mined citations for rs397516462 ...
HelpThese citations are identified by LitVar using
the rs number, so they may include citations for more than one variant
at this location. Please review the LitVar results carefully for your
variant of interest.
Record last updated May 01, 2024