NM_001004754.3(OR51I2):c.72C>G (p.His24Gln) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003265964.8
Allele description [Variation Report for NM_001004754.3(OR51I2):c.72C>G (p.His24Gln)]
NM_001004754.3(OR51I2):c.72C>G (p.His24Gln)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Apr 20, 2024