NM_198407.2(GHSR):c.78C>T (p.Gly26=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003662427.1
Allele description [Variation Report for NM_198407.2(GHSR):c.78C>T (p.Gly26=)]
NM_198407.2(GHSR):c.78C>T (p.Gly26=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024