NM_001018115.3(FANCD2):c.2605+1G>A AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 8, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000255506.3
Allele description [Variation Report for NM_001018115.3(FANCD2):c.2605+1G>A]
NM_001018115.3(FANCD2):c.2605+1G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 6, 2024