Annotation Detail
Information
- Associated Genes
- ALOX12 ALOX12-AS1
- Associated Variants
-
ALOX12 p.Leu634= (p.L634=)
(
ENST00000251535.11 )
ALOX12 p.Leu634= (p.L634=) ( ENST00000251535.11 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000697.3(ALOX12):c.1902G>A (p.Leu634=) AND not provided
- ClinVar Allele ID
- 1267551
- ClinVar RefSeq Alternation Syntax
- NM_000697.3:c.1902G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2021-06-09
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001687575
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs