NM_001034850.3(RETREG1):c.10C>T (p.Pro4Ser) 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:
- RCV001158111.4
Allele description [Variation Report for NM_001034850.3(RETREG1):c.10C>T (p.Pro4Ser)]
NM_001034850.3(RETREG1):c.10C>T (p.Pro4Ser)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024