NM_138711.6(PPARG):c.402G>T (p.Arg134=) AND PPARG-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 8, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004533560.1
Allele description [Variation Report for NM_138711.6(PPARG):c.402G>T (p.Arg134=)]
NM_138711.6(PPARG):c.402G>T (p.Arg134=)
Condition(s)
- Name:
- PPARG-related disorder
- Synonyms:
- PPARG-Related Disorders; PPARG-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Sep 16, 2024