NM_000514.4(GDNF):c.*1927C>T AND Hirschsprung disease, susceptibility to, 3
- 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:
- RCV000291626.5
Allele description [Variation Report for NM_000514.4(GDNF):c.*1927C>T]
NM_000514.4(GDNF):c.*1927C>T
Condition(s)
-
EVL Enah/Vasp-like [Homo sapiens]
EVL Enah/Vasp-like [Homo sapiens]Gene ID:51466Gene
-
Gene Links for GEO Profiles (Select 77280624) (1)
Gene
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Last Updated: Apr 9, 2023