Annotation Detail
Information
- Associated Genes
- LGALS2
- Associated Variants
-
LGALS2 c.6+3279C>T
(
ENST00000215886.6 )
LGALS2 c.6+3279C>T ( ENST00000215886.6 ) - Associated Disease
- Myocardial infarction, susceptibility to
- Source Database
- ClinVar
- Description
- NM_006498.3(LGALS2):c.6+3279C>T AND Myocardial infarction, susceptibility to
- ClinVar Allele ID
- 29511
- ClinVar RefSeq Alternation Syntax
- NM_006498.3:c.6+3279C>T
- Clinical Significance Description
- risk factor
- Clinical Significance Last Update
- 2004-05-06
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001799609
- ClinVar Disease
- Myocardial infarction, susceptibility to
- Observed Origin Sample
- germline
- Pubmed
- 15129282
Drugs