NM_022726.4(ELOVL4):c.*238_*242del AND Stargardt Disease, Dominant
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000396904.5
Allele description [Variation Report for NM_022726.4(ELOVL4):c.*238_*242del]
NM_022726.4(ELOVL4):c.*238_*242del
Condition(s)
- Name:
- Stargardt Disease, Dominant
- Identifiers:
- MedGen: CN239307
Assertion and evidence details
Last Updated: Apr 9, 2023