Annotation Detail
Information
- Associated Genes
- PRKG1 LOC124403957
- Associated Variants
-
GRCh38/hg38 10q21.1(chr10:52074749-52222855)x3
GRCh38/hg38 10q21.1(chr10:52074749-52222855)x3 - Source Database
- ClinVar
- Description
- GRCh38/hg38 10q21.1(chr10:52074749-52222855)x3 AND See cases
- ClinVar Allele ID
- 155458
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2010-11-30
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000135033
- Observed Origin Sample
- not provided
Drugs