NM_000458.4(HNF1B):c.-39A>C AND HNF1B-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 16, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003939427.1
Allele description [Variation Report for NM_000458.4(HNF1B):c.-39A>C]
NM_000458.4(HNF1B):c.-39A>C
Condition(s)
- Name:
- HNF1B-related disorder
- Synonyms:
- HNF1B-related condition; HNF1B-related disorders
- Identifiers:
Assertion and evidence details
Last Updated: May 19, 2024