GRCh37/hg19 14q32.11(chr14:91006120-91753359) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002052452.3
Allele description [Variation Report for GRCh37/hg19 14q32.11(chr14:91006120-91753359)]
GRCh37/hg19 14q32.11(chr14:91006120-91753359)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 15, 2022