NM_002016.2(FLG):c.6220G>C (p.Glu2074Gln) AND not provided
- Germline classification:
- Benign/Likely benign (5 submissions)
- Last evaluated:
- Dec 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001541191.14
Allele description [Variation Report for NM_002016.2(FLG):c.6220G>C (p.Glu2074Gln)]
NM_002016.2(FLG):c.6220G>C (p.Glu2074Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024