GRCh37/hg19 16p13.11(chr16:16248154-16258276)x1 AND See cases
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000448922.1
Allele description
GRCh37/hg19 16p13.11(chr16:16248154-16258276)x1
Condition(s)
- Name:
- See cases [See the Variation display for details]
- Identifiers:
Assertion and evidence details
Last Updated: Feb 20, 2022