NM_006623.4(PHGDH):c.792+6T>G AND not provided
- Germline classification:
- Benign/Likely benign (4 submissions)
- Last evaluated:
- Jul 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000518662.24
Allele description [Variation Report for NM_006623.4(PHGDH):c.792+6T>G]
NM_006623.4(PHGDH):c.792+6T>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024