NM_001122752.2(SERPINI1):c.-19+48C>T AND Familial encephalopathy with neuroserpin inclusion bodies
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000331710.5
Allele description [Variation Report for NM_001122752.2(SERPINI1):c.-19+48C>T]
NM_001122752.2(SERPINI1):c.-19+48C>T
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023