NM_002473.6(MYH9):c.5010G>A (p.Glu1670=) AND not specified
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Apr 30, 2012
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000155176.9
Allele description [Variation Report for NM_002473.6(MYH9):c.5010G>A (p.Glu1670=)]
NM_002473.6(MYH9):c.5010G>A (p.Glu1670=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024