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rs35569394

From SNPedia

Orientationplus
Stabilizedplus
Make rs35569394(-;-)
Make rs35569394(-;TCCCACTCTTCCCACAGG)
Make rs35569394(TCCCACTCTTCCCACAGG;TCCCACTCTTCCCACAGG)
ReferenceGRCh37.p2 37.2/134
Chromosome6
Position43736418
GeneVEGFA
is asnp
is mentioned by
dbSNPrs35569394
dbSNP (old)rs35569394
ClinGenrs35569394
ebirs35569394
HLIrs35569394
Exacrs35569394
Gnomadrs35569394
Varsomers35569394
Maprs35569394
PheGenIrs35569394
Biobankrs35569394
1000 genomesrs35569394
hgdprs35569394
ensemblrs35569394
gopubmedrs35569394
geneviewrs35569394
scholarrs35569394
googlers35569394
pharmgkbrs35569394
gwascentralrs35569394
openSNPrs35569394
23andMers35569394
23andMe allrs35569394
SNP Nexus

SNPshotrs35569394
SNPdbers35569394
MSV3drs35569394
GWAS Ctlgrs35569394
StatusDeleted
Max Magnitude

[PMID 19429179] Association between promoter polymorphisms of vascular endothelial growth factor gene and sporadic Alzheimer's disease among Northern Chinese Han

[PMID 20406100] The Vascular Endothelial Growth Factor-2549 Insertion/Deletion Polymorphism Is Not Associated with Susceptibility to Hepatocellular Carcinoma in Chinese


[PMID 19587357OA-icon.png] A systematic meta-analysis of genetic association studies for diabetic retinopathy.


[PMID 20706635OA-icon.png] Human genetics of diabetic retinopathy: current perspectives.


[PMID 21347390OA-icon.png] Genetics of VEGF serum variation in human isolated populations of cilento: importance of VEGF polymorphisms.


[PMID 25711033] [Association between inflanummatory gene polymorphisms and the risk of myocardial infarction]


[PMID 26662939] Genotype/allelic combinations as potential predictors of myocardial infarction.