NM_198129.4(LAMA3):c.6649A>G (p.Lys2217Glu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004407261.1
Allele description [Variation Report for NM_198129.4(LAMA3):c.6649A>G (p.Lys2217Glu)]
NM_198129.4(LAMA3):c.6649A>G (p.Lys2217Glu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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See more...Assertion and evidence details
Last Updated: May 7, 2024