Annotation Detail
Information
- Associated Genes
- PAK5 PARAL1 LOC126862969 LOC130065413 LOC130065414
- Associated Variants
-
GRCh38/hg38 20p12.2(chr20:9771030-9988151)x3
GRCh38/hg38 20p12.2(chr20:9771030-9988151)x3 - Source Database
- ClinVar
- Description
- GRCh38/hg38 20p12.2(chr20:9771030-9988151)x3 AND See cases
- ClinVar Allele ID
- 162247
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2011-04-30
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000141036
- Observed Origin Sample
- not provided
Drugs