NM_022168.4(IFIH1):c.2788A>C (p.Asn930His) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 13, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002534464.2
Allele description [Variation Report for NM_022168.4(IFIH1):c.2788A>C (p.Asn930His)]
NM_022168.4(IFIH1):c.2788A>C (p.Asn930His)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024