NM_019076.5(UGT1A8):c.855+63762T>G AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Nov 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001618721.21
Allele description [Variation Report for NM_019076.5(UGT1A8):c.855+63762T>G]
NM_019076.5(UGT1A8):c.855+63762T>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 9, 2024