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rs17045031

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs17045031(A;A)
Make rs17045031(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position66717940
is asnp
is mentioned by
dbSNPrs17045031
ebirs17045031
HLIrs17045031
Exacrs17045031
Varsomers17045031
Maprs17045031
PheGenIrs17045031
hapmaprs17045031
1000 genomesrs17045031
hgdprs17045031
ensemblrs17045031
gopubmedrs17045031
geneviewrs17045031
scholarrs17045031
googlers17045031
pharmgkbrs17045031
gwascentralrs17045031
openSNPrs17045031
23andMers17045031
23andMe allrs17045031
SNP Nexus

SNPshotrs17045031
SNPdbers17045031
MSV3drs17045031
GWAS Ctlgrs17045031
GMAF0.08999
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21909108OA-icon.png]
Trait
Title Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.
Risk Allele A
P-val 4E-7
Odds Ratio 0.2986 [0.18-0.42] unit decrease