rs699946

Orientation

plus

Stabilized

plus

Make rs699946(A;A)

Make rs699946(A;G)

Make rs699946(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

43764932

is a	snp
is	mentioned by
dbSNP	rs699946
dbSNP (classic)	rs699946
ClinGen	rs699946
ebi	rs699946
HLI	rs699946
Exac	rs699946
Gnomad	rs699946
Varsome	rs699946
LitVar	rs699946
Map	rs699946
PheGenI	rs699946
Biobank	rs699946
1000 genomes	rs699946
hgdp	rs699946
ensembl	rs699946
geneview	rs699946
scholar	rs699946
google	rs699946
pharmgkb	rs699946
gwascentral	rs699946
openSNP	rs699946
23andMe	rs699946
SNPshot	rs699946
SNPdbe	rs699946
MSV3d	rs699946
GWAS Ctlg	rs699946

GMAF

0.2576

Max Magnitude

0

?	(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 19308252] 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 24652518] VEGFA and VEGFR2 gene polymorphisms and response to anti-vascular endothelial growth factor therapy: comparison of age-related macular degeneration treatments trials (CATT)