NM_021614.4(KCNN2):c.2267T>G (p.Met756Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002920951.2
Allele description [Variation Report for NM_021614.4(KCNN2):c.2267T>G (p.Met756Arg)]
NM_021614.4(KCNN2):c.2267T>G (p.Met756Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 1, 2024