NM_022787.4(NMNAT1):c.606G>A (p.Val202=) AND Leber congenital amaurosis 9
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002701003.3
Allele description [Variation Report for NM_022787.4(NMNAT1):c.606G>A (p.Val202=)]
NM_022787.4(NMNAT1):c.606G>A (p.Val202=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024