GRCh37/hg19 7p22.3-22.2(chr7:2088540-3127784)x3 AND not specified
- 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:
- RCV003986692.1
Allele description [Variation Report for GRCh37/hg19 7p22.3-22.2(chr7:2088540-3127784)x3]
GRCh37/hg19 7p22.3-22.2(chr7:2088540-3127784)x3
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 30, 2024