NM_002473.6(MYH9):c.422A>G (p.Lys141Arg) AND MYH9-related disorder
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004544166.1
Allele description [Variation Report for NM_002473.6(MYH9):c.422A>G (p.Lys141Arg)]
NM_002473.6(MYH9):c.422A>G (p.Lys141Arg)
Condition(s)
- Name:
- MYH9-related disorder
- Identifiers:
- MedGen: C1854520
Assertion and evidence details
Last Updated: Aug 11, 2024