Annotation Detail
Information
- Associated Genes
- LINC02290 LOC126861968 LOC129390635 LOC129390636 LOC132090241
- Associated Variants
-
GRCh38/hg38 14q23.3(chr14:65909873-66374685)x3
GRCh38/hg38 14q23.3(chr14:65909873-66374685)x3 - Source Database
- ClinVar
- Description
- GRCh38/hg38 14q23.3(chr14:65909873-66374685)x3 AND See cases
- ClinVar Allele ID
- 164760
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2012-09-21
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000143073
- Observed Origin Sample
- not provided
Drugs