{{Rsnum
|rsid=1870377
|Gene=KDR
|Chromosome=4
|position=55106807
|Orientation=plus
|GMAF=0.2346
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=KDR
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 6.2 | 43.1 | 50.8
| HCB | 31.1 | 44.4 | 24.4
| JPT | 11.4 | 43.2 | 45.5
| YRI | 1.6 | 20.6 | 77.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 31.1 | 44.4 | 24.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19875757
|Title=Clinical relevance of vascular endothelial growth factor (VEGFA) and VEGF receptor (VEGFR2) gene polymorphism on the treatment outcome following imatinib therapy
}}

{{PMID Auto
|PMID=22015057
|Title=Single nucleotide polymorphism associations with response and toxic effects in patients with advanced renal-cell carcinoma treated with first-line sunitinib: a multicentre, observational, prospective study
}}

{{PMID Auto
|PMID=22129133
|Title=VEGFA and VEGFR2 genetic polymorphisms and survival in patients with diffuse large B cell lymphoma
}}

{{PMID Auto
|PMID=22507619
|Title=Association and interaction between dietary pattern and VEGF receptor-2 (VEGFR2) gene polymorphisms on blood lipids in Chinese Malaysian and Japanese adults
}}

{{PMID|18194558|OA=1
}} A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples.

{{PMID|20019880|OA=1
}} Polymorphisms in the VEGFA and VEGFR-2 genes and neovascular age-related macular degeneration.

{{PMID|20215856|OA=1
}} Genetic association of angiogenesis- and hypoxia-related gene polymorphisms with osteonecrosis of the femoral head.

{{PMID|20389299|OA=1
}} Pazopanib-induced hyperbilirubinemia is associated with Gilbert's syndrome UGT1A1 polymorphism.

{{PMID|21257617}} Association of polymorphisms/haplotypes of the genes encoding vascular endothelial growth factor and its KDR receptor with recurrent pregnancy loss.

{{GET Evidence
|gene=KDR
|aa_change=Gln472His
|aa_change_short=Q472H
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1870377
|overall_frequency_n=2075
|overall_frequency_d=10758
|overall_frequency=0.19288
|n_genomes=22
|n_genomes_annotated=0
|n_haplomes=25
|n_articles=0
|n_articles_annotated=0
|nblosum100=-1
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=23111153
|Title=Implication of VEGFR2 in systemic lupus erythematosus: a combined genetic and structural biological approach
}}

{{PMID Auto
|PMID=23566851
|Title=Association study between of Tie2/angiopoietin-2 and VEGF/KDR pathway gene polymorphisms and vascular malformations
}}

{{PMID Auto
|PMID=25123269
|Title=Genetic variants in the KDR gene is associated with the prognosis of transarterial chemoembolization treated hepatocellular carcinoma
}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}