NC_012920.1:m.8856G>A AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 29, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000224222.2
Allele description [Variation Report for NC_012920.1:m.8856G>A]
NC_012920.1:m.8856G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: May 24, 2022