NM_020376.4(PNPLA2):c.42C>T (p.Gly14=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 16, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000901807.3
Allele description [Variation Report for NM_020376.4(PNPLA2):c.42C>T (p.Gly14=)]
NM_020376.4(PNPLA2):c.42C>T (p.Gly14=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Oct 14, 2023