NM_134261.3(RORA):c.197-26458C>T AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 9, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002826746.2
Allele description [Variation Report for NM_134261.3(RORA):c.197-26458C>T]
NM_134261.3(RORA):c.197-26458C>T
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
leukocyte immunoglobulin-like receptor subfamily A member 6 isoform X4 [Homo sap...
leukocyte immunoglobulin-like receptor subfamily A member 6 isoform X4 [Homo sapiens]gi|2462569059|ref|XP_054178779.1|Protein
-
Barrett esophagus: endoscopic biopsies
Barrett esophagus: endoscopic biopsiesAccession: GDS4350GEO DataSets
-
Related DataSets for GEO Profiles (Select 83901601) (1)
GEO DataSets
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See more...Assertion and evidence details
Last Updated: May 1, 2024