RGD Annotation Report for Angelman syndromeRat Genome Database

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An association has been curated linking LOC129390678 and Angelman 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
The annotation has been inferred by association of genotype and phenotype with RGD:151663622 (Homo sapiens)
183 RGD objects have been annotated to Angelman syndrome (DOID:1932)
0 papers in RGD have been used to annotate LOC129390678
Curation Notes: ClinVar Annotator: match by term: Angelman syndrome

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