NM_001374828.1(ARID1B):c.612_632del (p.Gln208_Gln214del) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 6, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002455965.3
Allele description [Variation Report for NM_001374828.1(ARID1B):c.612_632del (p.Gln208_Gln214del)]
NM_001374828.1(ARID1B):c.612_632del (p.Gln208_Gln214del)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Jun 23, 2024