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rs1547651

From SNPedia

Orientationplus
Stabilizedplus
Make rs1547651(A;A)
Make rs1547651(A;T)
Make rs1547651(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position43762907
is asnp
is mentioned by
dbSNPrs1547651
ebirs1547651
HLIrs1547651
Exacrs1547651
Varsomers1547651
Maprs1547651
PheGenIrs1547651
hapmaprs1547651
1000 genomesrs1547651
hgdprs1547651
ensemblrs1547651
gopubmedrs1547651
geneviewrs1547651
scholarrs1547651
googlers1547651
pharmgkbrs1547651
gwascentralrs1547651
openSNPrs1547651
23andMers1547651
23andMe allrs1547651
SNP Nexus

SNPshotrs1547651
SNPdbers1547651
MSV3drs1547651
GWAS Ctlgrs1547651
GMAF0.1295
Max Magnitude
? (A;A) (A;T) (T;T) 28


[PMID 21316969] Polymorphisms of the vascular endothelial growth factor A gene and susceptibility to sporadic brain arteriovenous malformation in a Chinese population


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


[PMID 21706043OA-icon.png] Polymorphisms of VEGFA gene and susceptibility to hemorrhage risk of brain arteriovenous malformations in a Chinese population.


GET Evidence
rs1547651
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0625
summary