NM_000251.3(MSH2):c.2210+274T>G AND Lynch syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 5, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000076425.4
Allele description [Variation Report for NM_000251.3(MSH2):c.2210+274T>G]
NM_000251.3(MSH2):c.2210+274T>G
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
Assertion and evidence details
Last Updated: May 7, 2024