GRCh37/hg19 Xp11.4(chrX:38486618-38629433)x2 AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 31, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000847626.2
Allele description [Variation Report for GRCh37/hg19 Xp11.4(chrX:38486618-38629433)x2]
GRCh37/hg19 Xp11.4(chrX:38486618-38629433)x2
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Dec 11, 2022