NM_001283009.2(RTEL1):c.1761G>A (p.Pro587=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002413378.3
Allele description [Variation Report for NM_001283009.2(RTEL1):c.1761G>A (p.Pro587=)]
NM_001283009.2(RTEL1):c.1761G>A (p.Pro587=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024