GRCh37/hg19 16p11.2(chr16:29580021-30190029)x3 AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004442835.1
Allele description [Variation Report for GRCh37/hg19 16p11.2(chr16:29580021-30190029)x3]
GRCh37/hg19 16p11.2(chr16:29580021-30190029)x3
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024