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rs699946

From SNPedia

Orientationplus
Stabilizedplus
Make rs699946(A;A)
Make rs699946(A;G)
Make rs699946(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position43764932
is asnp
is mentioned by
dbSNPrs699946
ebirs699946
HLIrs699946
Exacrs699946
Varsomers699946
Maprs699946
PheGenIrs699946
hapmaprs699946
1000 genomesrs699946
hgdprs699946
ensemblrs699946
gopubmedrs699946
geneviewrs699946
scholarrs699946
googlers699946
pharmgkbrs699946
gwascentralrs699946
openSNPrs699946
23andMers699946
23andMe allrs699946
SNP Nexus

SNPshotrs699946
SNPdbers699946
MSV3drs699946
GWAS Ctlgrs699946
GMAF0.2576
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19553626] Common sequence variation in the VEGFA gene predicts risk of diabetic retinopathy


[PMID 22258388] Association of NOS2 and potential effect of VEGF, IL6, CCL2 and IL1RN polymorphisms and haplotypes on susceptibility to GCA--a simultaneous study of 130 potentially functional SNPs in 14 candidate genes


[PMID 19308252OA-icon.png] Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation.


[PMID 21744122] VEGF gene polymorphism and response to intravitreal bevacizumab and triple therapy in age-related macular degeneration.


[PMID 24652518OA-icon.png] VEGFA and VEGFR2 gene polymorphisms and response to anti-vascular endothelial growth factor therapy: comparison of age-related macular degeneration treatments trials (CATT)