NM_001493.3(GDI1):c.219T>C (p.Asn73=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000117138.14
Allele description [Variation Report for NM_001493.3(GDI1):c.219T>C (p.Asn73=)]
NM_001493.3(GDI1):c.219T>C (p.Asn73=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024