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rs4804146

From SNPedia

Orientationplus
Stabilizedplus
Make rs4804146(C;C)
Make rs4804146(C;T)
Make rs4804146(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position11145500
is asnp
is mentioned by
dbSNPrs4804146
ebirs4804146
HLIrs4804146
Exacrs4804146
Varsomers4804146
Maprs4804146
PheGenIrs4804146
hapmaprs4804146
1000 genomesrs4804146
hgdprs4804146
ensemblrs4804146
gopubmedrs4804146
geneviewrs4804146
scholarrs4804146
googlers4804146
pharmgkbrs4804146
gwascentralrs4804146
openSNPrs4804146
23andMers4804146
23andMe allrs4804146
SNP Nexus

SNPshotrs4804146
SNPdbers4804146
MSV3drs4804146
GWAS Ctlgrs4804146
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24386095OA-icon.png]
Trait Lipid traits
Title A genome wide association study identifies common variants associated with lipid levels in the Chinese population.
Risk Allele C
P-val 7E-6
Odds Ratio .05 mmol/L decrease