NM_020975.6(RET):c.548G>A (p.Gly183Asp) AND Hirschsprung disease, susceptibility to, 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003468818.1
Allele description [Variation Report for NM_020975.6(RET):c.548G>A (p.Gly183Asp)]
NM_020975.6(RET):c.548G>A (p.Gly183Asp)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024