NM_213655.5(WNK1):c.2653G>T (p.Val885Phe) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 2, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002451286.2
Allele description [Variation Report for NM_213655.5(WNK1):c.2653G>T (p.Val885Phe)]
NM_213655.5(WNK1):c.2653G>T (p.Val885Phe)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 7, 2024