GRCh37/hg19 Xp11.4(chrX:38486799-38634614)x2 AND See cases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 15, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000512292.2
Allele description [Variation Report for GRCh37/hg19 Xp11.4(chrX:38486799-38634614)x2]
GRCh37/hg19 Xp11.4(chrX:38486799-38634614)x2
Condition(s)
- Name:
- See cases [See the Variation display for details]
- Identifiers:
Assertion and evidence details
Last Updated: Apr 23, 2022