NM_001034850.3(RETREG1):c.*853G>A AND Neuropathy, hereditary sensory and autonomic, type 2B
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000371489.5
Allele description [Variation Report for NM_001034850.3(RETREG1):c.*853G>A]
NM_001034850.3(RETREG1):c.*853G>A
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023