NM_000338.3(SLC12A1):c.1652C>T (p.Thr551Ile) AND Bartter disease type 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002251235.1
Allele description [Variation Report for NM_000338.3(SLC12A1):c.1652C>T (p.Thr551Ile)]
NM_000338.3(SLC12A1):c.1652C>T (p.Thr551Ile)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023