NC_000019.10:g.7633434C>T AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 29, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000455543.12
Allele description [Variation Report for NC_000019.10:g.7633434C>T]
NC_000019.10:g.7633434C>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024