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rs17489268

From SNPedia

Orientationplus
Stabilizedplus
Make rs17489268(A;A)
Make rs17489268(A;T)
Make rs17489268(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position19994534
is asnp
is mentioned by
dbSNPrs17489268
ebirs17489268
HLIrs17489268
Exacrs17489268
Varsomers17489268
Maprs17489268
PheGenIrs17489268
hapmaprs17489268
1000 genomesrs17489268
hgdprs17489268
ensemblrs17489268
gopubmedrs17489268
geneviewrs17489268
scholarrs17489268
googlers17489268
pharmgkbrs17489268
gwascentralrs17489268
openSNPrs17489268
23andMers17489268
23andMe allrs17489268
SNP Nexus

SNPshotrs17489268
SNPdbers17489268
MSV3drs17489268
GWAS Ctlgrs17489268
GMAF0.2443
Max Magnitude
? (A;A) (A;T) (T;T) 28
Rs17489268
PubMed [PMID 17634449OA-icon.png]
Affy Probeset SNP_A-2109814
Affy Orientation same
On GW 5.0 1
Alleles A/B A/T
Ancestral T
Population Caucasian
Allele A
Case Freq.
Control Freq.
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.25
Disease Coronary artery disease (CAD)


Neighborrs17411031
Distance265

rs17489268 increases susceptibility to Coronary artery disease 1.25 times for carriers of the A allele [PMID 17634449OA-icon.png]

[PMID 20018038OA-icon.png] Evaluation of genetic risk scores for lipid levels using genome-wide markers in the Framingham Heart Study.

[PMID 20370913OA-icon.png] Genome-wide association analysis of total cholesterol and high-density lipoprotein cholesterol levels using the Framingham heart study data.