NM_001161352.2(KCNMA1):c.16G>A (p.Gly6Ser) AND Intellectual disability
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001252027.4
Allele description [Variation Report for NM_001161352.2(KCNMA1):c.16G>A (p.Gly6Ser)]
NM_001161352.2(KCNMA1):c.16G>A (p.Gly6Ser)
Condition(s)
- Name:
- Intellectual disability
- Synonyms:
- Intellectual functioning disability; intellectual disabilities; Intellectual developmental disorder
- Identifiers:
- MONDO: MONDO:0001071; MeSH: D008607; MedGen: C3714756; Human Phenotype Ontology: HP:0001249
Assertion and evidence details
Last Updated: Aug 4, 2024