NM_006118.4(HAX1):c.426G>A (p.Gly142=) AND Kostmann syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001504280.7
Allele description [Variation Report for NM_006118.4(HAX1):c.426G>A (p.Gly142=)]
NM_006118.4(HAX1):c.426G>A (p.Gly142=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024