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rs833052

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs833052(A;A)
Make rs833052(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position43755598
is asnp
is mentioned by
dbSNPrs833052
ebirs833052
HLIrs833052
Exacrs833052
Varsomers833052
Maprs833052
PheGenIrs833052
hapmaprs833052
1000 genomesrs833052
hgdprs833052
ensemblrs833052
gopubmedrs833052
geneviewrs833052
scholarrs833052
googlers833052
pharmgkbrs833052
gwascentralrs833052
openSNPrs833052
23andMers833052
23andMe allrs833052
SNP Nexus

SNPshotrs833052
SNPdbers833052
MSV3drs833052
GWAS Ctlgrs833052
GMAF0.1708
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 22315135] The single-nucleotide polymorphisms +936 C/T VEGF and -710 C/T VEGFR1 are associated with breast cancer protection in a Spanish population


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


GET Evidence
rs833052
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.882812
summary



[PMID 24940484OA-icon.png] Association between vascular endothelial growth factor gene polymorphisms and bladder cancer risk