rs2305948

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs2305948(C;T)

Make rs2305948(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

55113391

Gene

KDR

is a	snp
is	mentioned by
dbSNP	rs2305948
dbSNP (classic)	rs2305948
ClinGen	rs2305948
ebi	rs2305948
HLI	rs2305948
Exac	rs2305948
Gnomad	rs2305948
Varsome	rs2305948
LitVar	rs2305948
Map	rs2305948
PheGenI	rs2305948
Biobank	rs2305948
1000 genomes	rs2305948
hgdp	rs2305948
ensembl	rs2305948
geneview	rs2305948
scholar	rs2305948
google	rs2305948
pharmgkb	rs2305948
gwascentral	rs2305948
openSNP	rs2305948
23andMe	rs2305948
SNPshot	rs2305948
SNPdbe	rs2305948
MSV3d	rs2305948
GWAS Ctlg	rs2305948

GMAF

0.1313

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

[PMID 19520980] VEGF Receptor-2 Variants Are Associated With Susceptibility to Stroke and Recurrence

[PMID 19875757] Clinical relevance of vascular endothelial growth factor (VEGFA) and VEGF receptor (VEGFR2) gene polymorphism on the treatment outcome following imatinib therapy

[PMID 22015057] 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 22129133 ] VEGFA and VEGFR2 genetic polymorphisms and survival in patients with diffuse large B cell lymphoma

[PMID 19953880] [Association of variants in the vascular endothelial growth factor receptor 2 gene and the risk of hemorrhagic stroke].

[PMID 20019880 ] Polymorphisms in the VEGFA and VEGFR-2 genes and neovascular age-related macular degeneration.

[PMID 20389299 ] Pazopanib-induced hyperbilirubinemia is associated with Gilbert's syndrome UGT1A1 polymorphism.

[PMID 20401335 ] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

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

[PMID 21791631 ] Pharmacogenetic angiogenesis profiling for first-line Bevacizumab plus oxaliplatin-based chemotherapy in patients with metastatic colorectal cancer.

[PMID 22274884] Association between genetic variations of vascular endothelial growth factor receptor 2 and glioma in the Chinese Han population.

[PMID 23030506] SINGLE NUCLEOTIDE POLYMORPHISM AND SERUM LEVELS OF VEGFR2 ARE ASSOCIATED WITH AGE RELATED MACULAR DEGENERATION

[PMID 23111153] Implication of VEGFR2 in systemic lupus erythematosus: a combined genetic and structural biological approach

[PMID 23102494] Vascular endothelial growth factor family gene polymorphisms in preeclampsia in Sinhalese women in Sri-Lanka.

[PMID 24886133 ] Kinase insert domain receptor/vascular endothelial growth factor receptor 2 (KDR) genetic variation is associated with ovarian hyperstimulation syndrome

[PMID 25128838] Minor association of kinase insert domain-containing receptor gene polymorphism (rs2071559) with myocardial infarction in Caucasians with type 2 diabetes mellitus: Case-control cross-sectional study

ClinVar
Risk	rs2305948(T;T)
Alt	rs2305948(T;T)
Reference	Rs2305948(C;C)
Significance	Untested
Disease	not specified
Variation	info
Gene	KDR
CLNDBN	not specified
Reversed	0
HGVS	NC_000004.11:g.55979558C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000121308.1,

[PMID 26081139] Genetic Variations of Kinase Inserts Domain Receptor (KDR) Gene Are Associated with the Risk of Astrocytomas

[PMID 26254278 ] Impact of VEGF, VEGFR, PDGFR, HIF and ERCC1 gene polymorphisms on thymic malignancies outcome after thymectomy

[PMID 25182707] The relationship of kinase insert domain receptor gene polymorphisms and clinical outcome in advanced hepatocellular carcinoma patients treated with sorafenib

[PMID 27141535 ] Association of kinase insert domain-containing receptor (KDR) gene polymorphism/ haplotypes with recurrent spontaneous abortion and genetic structure.

[PMID 32997825] VEGFR2 and VEGFA polymorphism are not associated with an inferior prognosis in Caucasian patients with aggressive B-cell lymphoma.