NM_000251.2(MSH2):c.-118T>C 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:
- RCV000075980.14
Allele description [Variation Report for NM_000251.2(MSH2):c.-118T>C]
NM_000251.2(MSH2):c.-118T>C
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
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440820[uid] AND (alive[prop]) (0)
Gene
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Last Updated: Oct 13, 2024