Annotation Detail
Information
- Associated Genes
- FABP2
- Associated Variants
-
FABP2 p.Thr55Ala (p.T55A)
(
ENST00000274024.4 )
FABP2 p.Thr55Ala (p.T55A) ( ENST00000274024.4 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000134.4(FABP2):c.163A>G (p.Thr55Ala) AND not provided
- ClinVar Allele ID
- 31533
- ClinVar RefSeq Alternation Syntax
- NM_000134.4:c.163A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-11-11
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001650835
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs