RGD Annotation Report for Lynch syndrome 1Rat Genome Database

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An association has been curated linking CV96478 and Lynch syndrome 1 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
21 RGD objects have been annotated to Lynch syndrome 1 (DOID:0070271)
1 papers in RGD have been used to annotate CV96478
Curation Notes: ClinVar Annotator: match by term: Lynch syndrome 1
Original References(s): PMID:25525159 PMID:25741868 PMID:26333163 PMID:28492532 PMID:30998989 PMID:33357406

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