Annotation Detail
Information
- Associated Genes
- ZMYND11 DIP2C LOC106783507 LOC126860802 LOC126860803 LOC126860804 LOC126860805 LOC126860806 LOC126860807 LOC130003153 LOC130003154
- Associated Variants
-
GRCh38/hg38 10p15.3(chr10:248232-587589)x3
GRCh38/hg38 10p15.3(chr10:248232-587589)x3 - Source Database
- ClinVar
- Description
- GRCh38/hg38 10p15.3(chr10:248232-587589)x3 AND See cases
- ClinVar Allele ID
- 72447
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2011-08-12
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000051592
- Observed Origin Sample
- maternal
Drugs