NM_000336.3(SCNN1B):c.777-5T>C AND Autosomal recessive pseudohypoaldosteronism type 1
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000371088.2
Allele description
NM_000336.3(SCNN1B):c.777-5T>C
Condition(s)
Assertion and evidence details
Last Updated: Jan 1, 2022