NM_020975.6(RET):c.2418C>T (p.Tyr806=) AND Hirschsprung disease, susceptibility to, 1
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001104778.5
Allele description [Variation Report for NM_020975.6(RET):c.2418C>T (p.Tyr806=)]
NM_020975.6(RET):c.2418C>T (p.Tyr806=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 20, 2024