NM_006950.3(SYN1):c.1968G>A (p.Pro656=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 13, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002317657.9
Allele description [Variation Report for NM_006950.3(SYN1):c.1968G>A (p.Pro656=)]
NM_006950.3(SYN1):c.1968G>A (p.Pro656=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 8, 2024