RGD Annotation Report for Lynch syndromeRat Genome Database

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An association has been curated linking CV232732 and Lynch syndrome in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
136 RGD objects have been annotated to Lynch syndrome (DOID:3883)
1 papers in RGD have been used to annotate CV232732
Curation Notes: ClinVar Annotator: match by term: Hereditary nonpolyposis colorectal neoplasms
Original References(s): PMID:23621914 PMID:24608573 PMID:25503501 PMID:25741868 PMID:26467025 PMID:28492532 PMID:32095738

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.