NM_002693.3(POLG):c.3561G>C (p.Arg1187=) AND POLG-Related Spectrum Disorders
- Germline classification:
- Likely benign (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:
- RCV000388497.13
Allele description [Variation Report for NM_002693.3(POLG):c.3561G>C (p.Arg1187=)]
NM_002693.3(POLG):c.3561G>C (p.Arg1187=)
Condition(s)
- Name:
- POLG-Related Spectrum Disorders
- Identifiers:
- MedGen: C4763519
Assertion and evidence details
Last Updated: Jun 9, 2024