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rs17410962

From SNPedia

Orientationplus
Stabilizedplus
Make rs17410962(A;A)
Make rs17410962(A;G)
Make rs17410962(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position19990569
is asnp
is mentioned by
dbSNPrs17410962
dbSNP (classic)rs17410962
ClinGenrs17410962
ebirs17410962
HLIrs17410962
Exacrs17410962
Gnomadrs17410962
Varsomers17410962
LitVarrs17410962
Maprs17410962
PheGenIrs17410962
Biobankrs17410962
1000 genomesrs17410962
hgdprs17410962
ensemblrs17410962
geneviewrs17410962
scholarrs17410962
googlers17410962
pharmgkbrs17410962
gwascentralrs17410962
openSNPrs17410962
23andMers17410962
SNPshotrs17410962
SNPdbers17410962
MSV3drs17410962
GWAS Ctlgrs17410962
GMAF0.1488
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23726366OA-icon.png]
Trait Triglycerides
Title Genome-wide Characterization of Shared and Distinct Genetic Components that Influence Blood Lipid Levels in Ethnically Diverse Human Populations.
Risk Allele G
P-val 7E-9
Odds Ratio .11 [NR] unit decrease


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


[PMID 20018089OA-icon.png] Toward the identification of causal genes in complex diseases: a gene-centric joint test of significance combining genomic and transcriptomic data.


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