NM_020366.4(RPGRIP1):c.2100G>C (p.Arg700=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002205475.6
Allele description [Variation Report for NM_020366.4(RPGRIP1):c.2100G>C (p.Arg700=)]
NM_020366.4(RPGRIP1):c.2100G>C (p.Arg700=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024