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rs6921438

From SNPedia

Orientationplus
Stabilizedplus
Make rs6921438(A;A)
Make rs6921438(A;G)
Make rs6921438(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position43957870
is asnp
is mentioned by
dbSNPrs6921438
ebirs6921438
HLIrs6921438
Exacrs6921438
Varsomers6921438
Maprs6921438
PheGenIrs6921438
hapmaprs6921438
1000 genomesrs6921438
hgdprs6921438
ensemblrs6921438
gopubmedrs6921438
geneviewrs6921438
scholarrs6921438
googlers6921438
pharmgkbrs6921438
gwascentralrs6921438
openSNPrs6921438
23andMers6921438
23andMe allrs6921438
SNP Nexus

SNPshotrs6921438
SNPdbers6921438
MSV3drs6921438
GWAS Ctlgrs6921438
GMAF0.4559
Max Magnitude
? (A;A) (A;G) (G;G) 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 21757650OA-icon.png] Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels.