NM_015120.4(ALMS1):c.41_42insAGA (p.Glu29dup) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 30, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000610358.1
Allele description
NM_015120.4(ALMS1):c.41_42insAGA (p.Glu29dup)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 5, 2021