Annotation Detail
Information
- Associated Genes
- FOXL2 PIK3CB COPB2 MRPS22 PRR23B PRR23C FOXL2NB PRR23A
- Associated Variants
- GRCh37/hg19 3q22.3-23(chr3:138413416-139096053)x3
- Source Database
- ClinVar
- Description
- GRCh37/hg19 3q22.3-23(chr3:138413416-139096053)x3 AND See cases
- ClinVar Allele ID
- 436067
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2015-07-15
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000511927
- Observed Origin Sample
- not provided
Drugs