NM_025114.4(CEP290):c.6960+10G>A AND not specified
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Aug 24, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000434151.9
Allele description [Variation Report for NM_025114.4(CEP290):c.6960+10G>A]
NM_025114.4(CEP290):c.6960+10G>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024