NM_213655.5(WNK1):c.2659T>C (p.Leu887=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 11, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002431777.9
Allele description [Variation Report for NM_213655.5(WNK1):c.2659T>C (p.Leu887=)]
NM_213655.5(WNK1):c.2659T>C (p.Leu887=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Oct 20, 2024