GRCh37/hg19 16p13.3(chr16:6278880-7092135)x1 AND See cases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 26, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000512426.2
Allele description [Variation Report for GRCh37/hg19 16p13.3(chr16:6278880-7092135)x1]
GRCh37/hg19 16p13.3(chr16:6278880-7092135)x1
Condition(s)
- Name:
- See cases [See the Variation display for details]
- Identifiers:
Assertion and evidence details
Last Updated: Mar 26, 2023