NM_000249.4(MLH1):c.1732-3T>C AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001341182.2
Allele description [Variation Report for NM_000249.4(MLH1):c.1732-3T>C]
NM_000249.4(MLH1):c.1732-3T>C
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesMedGen
-
C0027612[conceptid] (1)
MedGen
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See more...Assertion and evidence details
Last Updated: May 7, 2024