NM_207034.3(EDN3):c.49G>A (p.Ala17Thr) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 6, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000222596.7
Allele description [Variation Report for NM_207034.3(EDN3):c.49G>A (p.Ala17Thr)]
NM_207034.3(EDN3):c.49G>A (p.Ala17Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 12, 2024