Annotation Detail
Information
- Associated Genes
- CETN3 MEF2C POLR3G ARRDC3 ADGRV1 LYSMD3 MBLAC2 TMEM161B MIR9-2 LUCAT1
- Associated Variants
- GRCh37/hg19 5q14.3-15(chr5:87399001-92675748)x3
- Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- GRCh37/hg19 5q14.3-15(chr5:87399001-92675748)x3 AND not provided
- ClinVar Allele ID
- 554271
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2017-08-22
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000682576
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs