NM_001106.4(ACVR2B):c.*9737C>T AND Heterotaxy, visceral, 4, autosomal
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000319822.5
Allele description [Variation Report for NM_001106.4(ACVR2B):c.*9737C>T]
NM_001106.4(ACVR2B):c.*9737C>T
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023