NM_018979.4(WNK1):c.2664A>G (p.Val888=) AND WNK1-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 15, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003979912.2
Allele description [Variation Report for NM_018979.4(WNK1):c.2664A>G (p.Val888=)]
NM_018979.4(WNK1):c.2664A>G (p.Val888=)
Condition(s)
- Name:
- WNK1-related disorder
- Synonyms:
- WNK1-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Nov 10, 2024