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rs1260333

From SNPedia

Orientationminus
Stabilizedminus
Make rs1260333(C;C)
Make rs1260333(C;T)
Make rs1260333(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position27525757
is asnp
is mentioned by
dbSNPrs1260333
ebirs1260333
HLIrs1260333
Exacrs1260333
Varsomers1260333
Maprs1260333
PheGenIrs1260333
hapmaprs1260333
1000 genomesrs1260333
hgdprs1260333
ensemblrs1260333
gopubmedrs1260333
geneviewrs1260333
scholarrs1260333
googlers1260333
pharmgkbrs1260333
gwascentralrs1260333
openSNPrs1260333
23andMers1260333
23andMe allrs1260333
SNP Nexus

SNPshotrs1260333
SNPdbers1260333
MSV3drs1260333
GWAS Ctlgrs1260333
GMAF0.4513
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 C
P-val 2E-19
Odds Ratio 0.05 [0.04-0.06] unit decrease


[PMID 18439548OA-icon.png] Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.


[PMID 18439552OA-icon.png] Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein.


[PMID 23832694] Common genetic variants associated with lipid profiles in a Chinese pediatric population.