NM_000251.3(MSH2):c.1937A>C (p.Asp646Ala) AND Lynch syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003998757.2
Allele description [Variation Report for NM_000251.3(MSH2):c.1937A>C (p.Asp646Ala)]
NM_000251.3(MSH2):c.1937A>C (p.Asp646Ala)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
-
Homo sapiens
Homo sapiensInteraction between retinol intake and ISX rs5755368 polymorphism in colorectal cancer risk: a case-control study in a Korean populationBioProject
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Last Updated: Sep 29, 2024