NM_198129.4(LAMA3):c.9574A>T (p.Thr3192Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002546015.2
Allele description [Variation Report for NM_198129.4(LAMA3):c.9574A>T (p.Thr3192Ser)]
NM_198129.4(LAMA3):c.9574A>T (p.Thr3192Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 16, 2024