NM_000251.3(MSH2):c.2308A>G (p.Ile770Val) AND Lynch syndrome
- Germline classification:
- Uncertain significance (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:
- RCV000076457.9
Allele description [Variation Report for NM_000251.3(MSH2):c.2308A>G (p.Ile770Val)]
NM_000251.3(MSH2):c.2308A>G (p.Ile770Val)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
Assertion and evidence details
Last Updated: Jul 23, 2024