NM_015272.5(RPGRIP1L):c.3616+7A>G AND Meckel syndrome, type 5
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001120152.4
Allele description [Variation Report for NM_015272.5(RPGRIP1L):c.3616+7A>G]
NM_015272.5(RPGRIP1L):c.3616+7A>G
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024