KDR, kinase insert domain receptor, 3791

N. diseases: 623; N. variants: 23
Disease: HEMANGIOMA, CAPILLARY INFANTILE ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121917766
rs121917766
Entrez Id: 3791
Gene Symbol: KDR
KDR
CUI: C1865871
Disease:
HEMANGIOMA, CAPILLARY INFANTILE 		0.800 GeneticVariation UNIPROT Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma. 18931684 2008
dbSNP: rs121917766
rs121917766
Entrez Id: 3791
Gene Symbol: KDR
KDR
CUI: C1865871
Disease:
HEMANGIOMA, CAPILLARY INFANTILE 		0.800 GeneticVariation UNIPROT Patterns of somatic mutation in human cancer genomes. 17344846 2007
dbSNP: rs121917766
rs121917766
Entrez Id: 3791
Gene Symbol: KDR
KDR
CUI: C1865871
Disease:
HEMANGIOMA, CAPILLARY INFANTILE 		0.800 GeneticVariation UNIPROT Somatic mutation of vascular endothelial growth factor receptors in juvenile hemangioma. 11807987 2002
dbSNP: rs121917766
rs121917766
Entrez Id: 3791
Gene Symbol: KDR
KDR
CUI: C1865871
Disease:
HEMANGIOMA, CAPILLARY INFANTILE 		A 0.800 CausalMutation CLINVAR