NM_000539.3(RHO):c.696+4C>T AND Congenital stationary night blindness autosomal dominant 1
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000262697.5
Allele description [Variation Report for NM_000539.3(RHO):c.696+4C>T]
NM_000539.3(RHO):c.696+4C>T
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024