NM_001346754.2(PIGW):c.58C>T (p.Leu20=) AND Hyperphosphatasia with intellectual disability syndrome 5
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 3, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002176581.5
Allele description [Variation Report for NM_001346754.2(PIGW):c.58C>T (p.Leu20=)]
NM_001346754.2(PIGW):c.58C>T (p.Leu20=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024