GRCh37/hg19 Xp11.4(chrX:38480079-38634614) 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:
- RCV003986229.1
Allele description [Variation Report for GRCh37/hg19 Xp11.4(chrX:38480079-38634614)]
GRCh37/hg19 Xp11.4(chrX:38480079-38634614)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 30, 2024