NM_022726.4(ELOVL4):c.895A>G (p.Met299Val) AND Stargardt disease 3
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jul 30, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000305578.15
Allele description [Variation Report for NM_022726.4(ELOVL4):c.895A>G (p.Met299Val)]
NM_022726.4(ELOVL4):c.895A>G (p.Met299Val)
Condition(s)
Assertion and evidence details
Last Updated: Apr 20, 2024