NM_002299.4(LCT):c.5768C>A (p.Pro1923Gln) AND LCT-related disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 8, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003972396.2
Allele description [Variation Report for NM_002299.4(LCT):c.5768C>A (p.Pro1923Gln)]
NM_002299.4(LCT):c.5768C>A (p.Pro1923Gln)
Condition(s)
- Name:
- LCT-related disorder
- Synonyms:
- LCT-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Oct 8, 2024