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rs4938303

From SNPedia

Orientationplus
Stabilizedplus
Make rs4938303(C;C)
Make rs4938303(C;T)
Make rs4938303(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116714271
is asnp
is mentioned by
dbSNPrs4938303
ebirs4938303
HLIrs4938303
Exacrs4938303
Varsomers4938303
Maprs4938303
PheGenIrs4938303
hapmaprs4938303
1000 genomesrs4938303
hgdprs4938303
ensemblrs4938303
gopubmedrs4938303
geneviewrs4938303
scholarrs4938303
googlers4938303
pharmgkbrs4938303
gwascentralrs4938303
openSNPrs4938303
23andMers4938303
23andMe allrs4938303
SNP Nexus

SNPshotrs4938303
SNPdbers4938303
MSV3drs4938303
GWAS Ctlgrs4938303
GMAF0.4082
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20864672OA-icon.png]
Trait
Title Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
Risk Allele T
P-val 4E-21
Odds Ratio 0.07 [0.06-0.08] unit decrease