NM_018979.4(WNK1):c.6021A>G (p.Leu2007=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002227371.7
Allele description [Variation Report for NM_018979.4(WNK1):c.6021A>G (p.Leu2007=)]
NM_018979.4(WNK1):c.6021A>G (p.Leu2007=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024