Annotation Detail
Information
- Associated Genes
- OR2J2 LOC126859636
- Associated Variants
-
GRCh38/hg38 6p22.1(chr6:29134533-29184989)x3
GRCh38/hg38 6p22.1(chr6:29134533-29184989)x3 - Source Database
- ClinVar
- Description
- GRCh38/hg38 6p22.1(chr6:29134533-29184989)x3 AND See cases
- ClinVar Allele ID
- 162165
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2011-04-30
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000140955
- Observed Origin Sample
- not provided
Drugs