NM_001025295.3(IFITM5):c.34G>T (p.Ala12Ser) AND Osteogenesis imperfecta
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 9, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002277007.3
Allele description [Variation Report for NM_001025295.3(IFITM5):c.34G>T (p.Ala12Ser)]
NM_001025295.3(IFITM5):c.34G>T (p.Ala12Ser)
Condition(s)
Assertion and evidence details
Last Updated: Oct 8, 2024