NM_173076.3(ABCA12):c.2868T>G (p.Val956=) AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000892356.18
Allele description [Variation Report for NM_173076.3(ABCA12):c.2868T>G (p.Val956=)]
NM_173076.3(ABCA12):c.2868T>G (p.Val956=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024