NM_000392.5(ABCC2):c.2748-13T>G AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 27, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003872368.1
Allele description [Variation Report for NM_000392.5(ABCC2):c.2748-13T>G]
NM_000392.5(ABCC2):c.2748-13T>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024