NM_003863.3(DPM2):c.-429G>T AND Congenital muscular dystrophy with intellectual disability and severe epilepsy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000288874.14
Allele description [Variation Report for NM_003863.3(DPM2):c.-429G>T]
NM_003863.3(DPM2):c.-429G>T
Condition(s)
Assertion and evidence details
Last Updated: Mar 23, 2024