Annotation Detail
Information
- Associated Genes
- LPAR2
- Associated Variants
-
LPAR2 p.Thr233Met (p.T233M)
(
ENST00000407877.8,
ENST00000542587.5,
ENST00000586703.1 )
LPAR2 p.Thr233Met (p.T233M) ( ENST00000407877.8, ENST00000542587.5, ENST00000586703.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_004720.6(LPAR2):c.707C>T (p.Thr236Met) AND not provided
- ClinVar Allele ID
- 716318
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2019-12-31
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000973224
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs