NM_024757.5(EHMT1):c.2712+1G>C AND not provided
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000480859.1
Allele description [Variation Report for NM_024757.5(EHMT1):c.2712+1G>C]
NM_024757.5(EHMT1):c.2712+1G>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Jun 10, 2023