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VARIANT - TERM ANNOTATION REPORT

RGD ID: 8597407
Species: Homo sapiens
RGD Object: Variant
Symbol: CV22207
Name: NM_000492.4(CFTR):c.1766+1G>A
Acc ID: DOID:9008999
Term: Hereditary Pancreatitis
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.
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