Annotation Detail
Information
- Associated Genes
- N4BP3 NHP2 RMND5B LOC116158535 LOC121740634 LOC129995403 LOC129995404 LOC129995405 LOC129995406 LOC129995407 LOC129995408 LOC129995409 LOC129995410 LOC129995411
- Associated Variants
-
GRCh38/hg38 5q35.3(chr5:178021540-178160440)x3
GRCh38/hg38 5q35.3(chr5:178021540-178160440)x3 - Source Database
- ClinVar
- Description
- GRCh38/hg38 5q35.3(chr5:178021540-178160440)x3 AND See cases
- ClinVar Allele ID
- 161375
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2011-04-30
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000140328
- Observed Origin Sample
- not provided
Drugs