NM_198578.4(LRRK2):c.3325C>T (p.Leu1109=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 4, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002326416.2
Allele description [Variation Report for NM_198578.4(LRRK2):c.3325C>T (p.Leu1109=)]
NM_198578.4(LRRK2):c.3325C>T (p.Leu1109=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
txid1701393[Organism] (77)
Protein
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Last Updated: May 1, 2024