NM_005120.3(MED12):c.6208CAG[6] (p.Gln2076del) AND FG syndrome 1
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 27, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000459087.10
Allele description
NM_005120.3(MED12):c.6208CAG[6] (p.Gln2076del)
Condition(s)
Assertion and evidence details
Last Updated: Aug 5, 2023