NM_001379500.1(COL18A1):c.1221+14T>C AND Knobloch syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000301577.5
Allele description [Variation Report for NM_001379500.1(COL18A1):c.1221+14T>C]
NM_001379500.1(COL18A1):c.1221+14T>C
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024