NM_000088.4(COL1A1):c.1669-31T>C AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 7, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001000206.8
Allele description [Variation Report for NM_000088.4(COL1A1):c.1669-31T>C]
NM_000088.4(COL1A1):c.1669-31T>C
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Dec 24, 2023