NM_000179.3(MSH6):c.2668G>C (p.Val890Leu) AND Lynch syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 8, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003995423.2
Allele description [Variation Report for NM_000179.3(MSH6):c.2668G>C (p.Val890Leu)]
NM_000179.3(MSH6):c.2668G>C (p.Val890Leu)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
-
12119407[uid] (0)
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Last Updated: Sep 29, 2024