RGD Annotation Report for Meckel syndrome 2Rat Genome Database

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An association has been curated linking CV254217 and Meckel syndrome 2 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 Meckel syndrome 2 (DOID:0070116)
0 papers in RGD have been used to annotate CV254217
Curation Notes: ClinVar Annotator: match by term: Meckel syndrome, type 2
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.