NM_001072.4(UGT1A6):c.862-8101C>T AND UGT1A1-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 16, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004539218.1
Allele description [Variation Report for NM_001072.4(UGT1A6):c.862-8101C>T]
NM_001072.4(UGT1A6):c.862-8101C>T
Condition(s)
- Name:
- UGT1A1-related disorder
- Synonyms:
- UGT1A1-Related Disorders; UGT1A1-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Jul 7, 2024