NM_006772.3(SYNGAP1):c.1387-8G>A AND Intellectual disability, autosomal dominant 5
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 13, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001071926.7
Allele description [Variation Report for NM_006772.3(SYNGAP1):c.1387-8G>A]
NM_006772.3(SYNGAP1):c.1387-8G>A
Condition(s)
-
eggc.vip4Y2 (0)
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Last Updated: May 1, 2024