RGD Annotation Report for Finnish type amyloidosisRat Genome Database

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An association has been curated linking CV1479210 and Finnish type amyloidosis 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
1 RGD objects have been annotated to Finnish type amyloidosis (DOID:0050637)
0 papers in RGD have been used to annotate CV1479210
Curation Notes: ClinVar Annotator: match by term: Meretoja syndrome
Original References(s): PMID:25741868 PMID:28492532

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