NM_001543.5(NDST1):c.39C>G (p.His13Gln) AND Intellectual disability, autosomal recessive 46
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 11, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000678273.2
Allele description [Variation Report for NM_001543.5(NDST1):c.39C>G (p.His13Gln)]
NM_001543.5(NDST1):c.39C>G (p.His13Gln)
Condition(s)
Assertion and evidence details
Last Updated: Aug 5, 2023