GRCh37/hg19 9p21.2(chr9:25606107-25878901)x1 AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 2, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000748328.2
Allele description
GRCh37/hg19 9p21.2(chr9:25606107-25878901)x1
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Mar 4, 2023