Annotation Detail
Information
- Associated Genes
- PPP4R1 RAB31
- Associated Variants
- GRCh37/hg19 18p11.22(chr18:9550555-9833631)x3
- Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- GRCh37/hg19 18p11.22(chr18:9550555-9833631)x3 AND not provided
- ClinVar Allele ID
- 555686
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2018-05-04
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000683991
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs