RGD Annotation Report for sudden infant death syndromeRat Genome Database

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An association has been curated linking CV393753 and sudden infant death 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
42 RGD objects have been annotated to sudden infant death syndrome (DOID:9007)
0 papers in RGD have been used to annotate CV393753
Curation Notes: ClinVar Annotator: match by term: Sudden Infant Death
Original References(s): PMID:25741868 PMID:27485560 PMID:28492532 PMID:29895855

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