GRCh37/hg19 2p16.3(chr2:50964034-51915187) AND not specified
- Germline classification:
- Pathogenic (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:
- RCV002052626.3
Allele description [Variation Report for GRCh37/hg19 2p16.3(chr2:50964034-51915187)]
GRCh37/hg19 2p16.3(chr2:50964034-51915187)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 15, 2022