NM_000458.4(HNF1B):c.-23C>T AND HNF1B-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003896716.2
Allele description [Variation Report for NM_000458.4(HNF1B):c.-23C>T]
NM_000458.4(HNF1B):c.-23C>T
Condition(s)
- Name:
- HNF1B-related disorder
- Synonyms:
- HNF1B-related condition; HNF1B-related disorders
- Identifiers:
Assertion and evidence details
Last Updated: Oct 13, 2024