Annotation Detail
Information
- Associated Genes
- LPA
- Associated Variants
-
LPA c.3947+467T>C
(
ENST00000316300.10 )
LPA c.3947+467T>C ( ENST00000316300.10 ) - Associated Disease
- LIPOPROTEIN(a) POLYMORPHISM
- Source Database
- ClinVar
- Description
- NM_005577.4(LPA):c.3947+467T>C AND LIPOPROTEIN(a) POLYMORPHISM
- ClinVar Allele ID
- 227756
- ClinVar RefSeq Alternation Syntax
- NM_005577.4:c.3947+467T>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2020-08-07
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001251438
- ClinVar Disease
- LIPOPROTEIN(a) POLYMORPHISM
- Observed Origin Sample
- germline
- Pubmed
- 20032323
- Pubmed
- 23388002
Drugs