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VARIANT - TERM ANNOTATION REPORT

RGD ID: 156369914
Species: Homo sapiens
RGD Object: Variant
Symbol: CV2109674
Name: NM_003824.4(FADD):c.541C>G (p.Gln181Glu)
Acc ID: DOID:9003840
Term: Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations
Definition: null
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
CV2109674 IAGP 8554872ClinVarClinVar Annotator: match by term: Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformationsPMID:28492532
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