NM_016492.5(RANGRF):c.194+17C>G AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 18, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001718086.11
Allele description [Variation Report for NM_016492.5(RANGRF):c.194+17C>G]
NM_016492.5(RANGRF):c.194+17C>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 2, 2024