NM_001376.5(DYNC1H1):c.9469-20A>T AND not specified
- Germline classification:
- Benign (4 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000249467.10
Allele description [Variation Report for NM_001376.5(DYNC1H1):c.9469-20A>T]
NM_001376.5(DYNC1H1):c.9469-20A>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024