RGD Annotation Report for Brugada syndrome 8Rat Genome Database

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An association has been curated linking CV188642 and Brugada syndrome 8 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
10 RGD objects have been annotated to Brugada syndrome 8 (DOID:0110225)
1 papers in RGD have been used to annotate CV188642
Curation Notes: ClinVar Annotator: match by term: Brugada syndrome 8
Original References(s): PMID:25741868 PMID:28492532 PMID:28803248 PMID:29255176

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