NM_002693.3(POLG):c.2028G>A (p.Ala676=) AND POLG-Related Spectrum Disorders
- 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:
- RCV000263177.6
Allele description [Variation Report for NM_002693.3(POLG):c.2028G>A (p.Ala676=)]
NM_002693.3(POLG):c.2028G>A (p.Ala676=)
Condition(s)
- Name:
- POLG-Related Spectrum Disorders
- Identifiers:
- MedGen: C4763519
Assertion and evidence details
Last Updated: Apr 15, 2024