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rs515135

From SNPedia

Orientationminus
Stabilizedplus
Make rs515135(A;A)
Make rs515135(A;G)
Make rs515135(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position21063185
is asnp
is mentioned by
dbSNPrs515135
ebirs515135
HLIrs515135
Exacrs515135
Varsomers515135
Maprs515135
PheGenIrs515135
hapmaprs515135
1000 genomesrs515135
hgdprs515135
ensemblrs515135
gopubmedrs515135
geneviewrs515135
scholarrs515135
googlers515135
pharmgkbrs515135
gwascentralrs515135
openSNPrs515135
23andMers515135
23andMe allrs515135
SNP Nexus

SNPshotrs515135
SNPdbers515135
MSV3drs515135
GWAS Ctlgrs515135
GMAF0.2433
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20864672OA-icon.png]
Trait LDL cholesterol
Title Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
Risk Allele A
P-val 2E-20
Odds Ratio 0.04 [0.03-0.05] unit decrease
GWAS snp
PMID [PMID 19060906OA-icon.png]
Trait LDL cholesterol
Title Common variants at 30 loci contribute to polygenic dyslipidemia
Risk Allele T
P-val 5E-29
Odds Ratio 0.16 [0.12-0.20] SD decrease


[PMID 23202125OA-icon.png] Large-scale association analysis identifies new risk loci for coronary artery disease.

[PMID 23098650] Impact of variants within seven candidate genes on statin treatment efficacy

[PMID 19951432OA-icon.png] Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease.

GET Evidence
rs515135
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.710938
summary