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rs10738760

From SNPedia

Orientationplus
Stabilizedplus
Make rs10738760(A;A)
Make rs10738760(A;G)
Make rs10738760(G;G)
ReferenceGRCh37.p2 37.2/134
Chromosome9
Position2691186
is asnp
is mentioned by
dbSNPrs10738760
ebirs10738760
HLIrs10738760
Exacrs10738760
Varsomers10738760
Maprs10738760
PheGenIrs10738760
hapmaprs10738760
1000 genomesrs10738760
hgdprs10738760
ensemblrs10738760
gopubmedrs10738760
geneviewrs10738760
scholarrs10738760
googlers10738760
pharmgkbrs10738760
gwascentralrs10738760
openSNPrs10738760
23andMers10738760
23andMe allrs10738760
SNP Nexus

SNPshotrs10738760
SNPdbers10738760
MSV3drs10738760
GWAS Ctlgrs10738760
GMAF0.433
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21757650OA-icon.png]
Trait
Title Identification of cis- and trans-Acting Genetic Variants Explaining Up to Half the Variation in Circulating Vascular Endothelial Growth Factor Levels.
Risk Allele A
P-val 1E-39
Odds Ratio None None


[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