rs34255532, FLT4

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
HEMANGIOMA, CAPILLARY INFANTILE
CUI: C1865871
Disease: HEMANGIOMA, CAPILLARY INFANTILE
0.700 GeneticVariation UNIPROT
Hemangioma
CUI: C0018916
Disease: Hemangioma
0.010 GeneticVariation BEFREE Mutations were found in two of the 15 hemangioma specimens: a missense mutation (P1147S) in the kinase domain of the VEGFR2 (FLK1/KDR) gene in one specimen and a missense mutation (P954S) in the kinase insert of the VEGFR3 (FLT4) gene in another specimen. 11807987 2002