NM_000037.4(ANK1):c.3486C>T (p.Ser1162=) AND Hereditary spherocytosis type 1
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Nov 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000407847.18
Allele description [Variation Report for NM_000037.4(ANK1):c.3486C>T (p.Ser1162=)]
NM_000037.4(ANK1):c.3486C>T (p.Ser1162=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 10, 2024