Variant Term Annotation Report - Rat Genome Database

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VARIANT - TERM ANNOTATION REPORT

RGD ID:	12891537
Species:	Homo sapiens
RGD Object:	Variant
Symbol:	CV403702
Name:	NC_000021.9:g.(?_34787801)_(35048958_?)del

Acc ID:	DOID:9003178
Term:	Familial Platelet Disorder with Associated Myeloid Malignancy
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 Symbol	Qualifier	Evidence	With	Reference	Source	Notes	Original Reference(s)
CV403702		IAGP		8554872	ClinVar	ClinVar Annotator: match by term: Familial platelet disorder with associated myeloid malignancy	PMID:28492532

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