NM_005502.4(ABCA1):c.5376C>T (p.Thr1792=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 25, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001731637.1
Allele description [Variation Report for NM_005502.4(ABCA1):c.5376C>T (p.Thr1792=)]
NM_005502.4(ABCA1):c.5376C>T (p.Thr1792=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024