GRCh37/hg19 8p23.3(chr8:1832844-1838287)x0 AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 1, 2011
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000747270.2
Allele description [Variation Report for GRCh37/hg19 8p23.3(chr8:1832844-1838287)x0]
GRCh37/hg19 8p23.3(chr8:1832844-1838287)x0
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Mar 26, 2023