Annotation Detail
Information
- Associated Genes
- FAAH
- Associated Variants
-
FAAH p.Pro129Thr (p.P129T)
(
ENST00000243167.9 )
FAAH p.Pro129Thr (p.P129T) ( ENST00000243167.9 ) - Associated Disease
- FAAH POLYMORPHISM
- Source Database
- ClinVar
- Description
- NM_001441.3(FAAH):c.385C>A (p.Pro129Thr) AND FAAH POLYMORPHISM
- ClinVar Allele ID
- 21763
- ClinVar RefSeq Alternation Syntax
- NM_001441.3:c.385C>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2013-04-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000007116
- ClinVar Disease
- FAAH POLYMORPHISM
- Observed Origin Sample
- germline
- Pubmed
- 12060782
- Pubmed
- 15254019
- Pubmed
- 16972078
- Pubmed
- 23556448
Drugs