NM_002299.4(LCT):c.729C>G (p.Val243=) AND Lactose intolerance
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000333068.5
Allele description [Variation Report for NM_002299.4(LCT):c.729C>G (p.Val243=)]
NM_002299.4(LCT):c.729C>G (p.Val243=)
Condition(s)
- Name:
- Lactose intolerance
- Identifiers:
- MONDO: MONDO:0100345; MedGen: C0022951; Human Phenotype Ontology: HP:0004789
Assertion and evidence details
Last Updated: Sep 29, 2024