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rs12449157

From SNPedia

Orientationplus
Stabilizedplus
Make rs12449157(A;A)
Make rs12449157(A;G)
Make rs12449157(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position67674994
GeneGFOD2
is asnp
is mentioned by
dbSNPrs12449157
dbSNP (classic)rs12449157
ClinGenrs12449157
ebirs12449157
HLIrs12449157
Exacrs12449157
Gnomadrs12449157
Varsomers12449157
LitVarrs12449157
Maprs12449157
PheGenIrs12449157
Biobankrs12449157
1000 genomesrs12449157
hgdprs12449157
ensemblrs12449157
geneviewrs12449157
scholarrs12449157
googlers12449157
pharmgkbrs12449157
gwascentralrs12449157
openSNPrs12449157
23andMers12449157
SNPshotrs12449157
SNPdbers12449157
MSV3drs12449157
GWAS Ctlgrs12449157
GMAF0.2663
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 20864672OA-icon.png]
Trait
Title Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
Risk Allele G
P-val 2E-7
Odds Ratio 0.02 [0.01-0.03] unit increase