GRCh37/hg19 Xp22.33(chrX:3296723-3880686)x2 AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001829109.1
Allele description [Variation Report for GRCh37/hg19 Xp22.33(chrX:3296723-3880686)x2]
GRCh37/hg19 Xp22.33(chrX:3296723-3880686)x2
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 23, 2022