Annotation Detail
Information
- Associated Genes
- LOC129992316 LOC129992317 LOC129992318
- Associated Variants
-
GRCh38/hg38 4p15.31(chr4:18360417-19175273)x3
GRCh38/hg38 4p15.31(chr4:18360417-19175273)x3 - Source Database
- ClinVar
- Description
- GRCh38/hg38 4p15.31(chr4:18360417-19175273)x3 AND See cases
- ClinVar Allele ID
- 156295
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2010-12-22
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000135815
- Observed Origin Sample
- paternal
Drugs