NM_032578.4(MYPN):c.2925+9G>C AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001812101.16
Allele description [Variation Report for NM_032578.4(MYPN):c.2925+9G>C]
NM_032578.4(MYPN):c.2925+9G>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 9, 2024