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rs10489615

From SNPedia

Orientationplus
Stabilizedplus
Make rs10489615(A;A)
Make rs10489615(A;G)
Make rs10489615(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position230169242
GeneGALNT2
is asnp
is mentioned by
dbSNPrs10489615
ebirs10489615
HLIrs10489615
Exacrs10489615
Varsomers10489615
Maprs10489615
PheGenIrs10489615
hapmaprs10489615
1000 genomesrs10489615
hgdprs10489615
ensemblrs10489615
gopubmedrs10489615
geneviewrs10489615
scholarrs10489615
googlers10489615
pharmgkbrs10489615
gwascentralrs10489615
openSNPrs10489615
23andMers10489615
23andMe allrs10489615
SNP Nexus

SNPshotrs10489615
SNPdbers10489615
MSV3drs10489615
GWAS Ctlgrs10489615
GMAF0.4284
Max Magnitude
? (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 4E-9
Odds Ratio 0.02 [0.01-0.03] unit increase