NM_198578.4(LRRK2):c.3477T>C (p.Ser1159=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 28, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002457334.1
Allele description [Variation Report for NM_198578.4(LRRK2):c.3477T>C (p.Ser1159=)]
NM_198578.4(LRRK2):c.3477T>C (p.Ser1159=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Apr 15, 2023