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rs4416670

From SNPedia

Orientationplus
Stabilizedplus
Make rs4416670(C;C)
Make rs4416670(C;T)
Make rs4416670(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position43982716
is asnp
is mentioned by
dbSNPrs4416670
ebirs4416670
HLIrs4416670
Exacrs4416670
Varsomers4416670
Maprs4416670
PheGenIrs4416670
hapmaprs4416670
1000 genomesrs4416670
hgdprs4416670
ensemblrs4416670
gopubmedrs4416670
geneviewrs4416670
scholarrs4416670
googlers4416670
pharmgkbrs4416670
gwascentralrs4416670
openSNPrs4416670
23andMers4416670
23andMe allrs4416670
SNP Nexus

SNPshotrs4416670
SNPdbers4416670
MSV3drs4416670
GWAS Ctlgrs4416670
GMAF0.4633
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23204297OA-icon.png] A common variant highly associated with plasma VEGFA levels also contributes to the variation of both LDL-C and HDL-C

[PMID 23201487] Associations of vascular endothelial growth factor (VEGF) with adhesion and inflammation molecules in a healthy population [PMID 21757650OA-icon.png] Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels.