NM_001371596.2(MFSD8):c.998+17T>G AND Neuronal ceroid lipofuscinosis 7
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003496673.2
Allele description [Variation Report for NM_001371596.2(MFSD8):c.998+17T>G]
NM_001371596.2(MFSD8):c.998+17T>G
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024