GRCh37/hg19 10q26.13-26.3(chr10:126914469-135427143)x1 AND See cases
- Germline classification:
- Pathogenic (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002292397.1
Allele description [Variation Report for GRCh37/hg19 10q26.13-26.3(chr10:126914469-135427143)x1]
GRCh37/hg19 10q26.13-26.3(chr10:126914469-135427143)x1
Condition(s)
- Name:
- See cases [See the Variation display for details]
- Identifiers:
-
C4749042[trait identifier] AND "Fulgent Genetics, Fulgent Genetic... (1)
C4749042[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[submitter]SearchClinVar
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See more...Assertion and evidence details
Last Updated: Oct 22, 2022