GRCh37/hg19 9p22.1(chr9:18935985-19603778)x3 AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 14, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000683139.1
Allele description [Variation Report for GRCh37/hg19 9p22.1(chr9:18935985-19603778)x3]
GRCh37/hg19 9p22.1(chr9:18935985-19603778)x3
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 23, 2022