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rs17398575

From SNPedia

Orientationplus
Stabilizedplus
Make rs17398575(A;A)
Make rs17398575(A;G)
Make rs17398575(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position106769006
is asnp
is mentioned by
dbSNPrs17398575
ebirs17398575
HLIrs17398575
Exacrs17398575
Varsomers17398575
Maprs17398575
PheGenIrs17398575
hapmaprs17398575
1000 genomesrs17398575
hgdprs17398575
ensemblrs17398575
gopubmedrs17398575
geneviewrs17398575
scholarrs17398575
googlers17398575
pharmgkbrs17398575
gwascentralrs17398575
openSNPrs17398575
23andMers17398575
23andMe allrs17398575
SNP Nexus

SNPshotrs17398575
SNPdbers17398575
MSV3drs17398575
GWAS Ctlgrs17398575
GMAF0.1639
Max Magnitude
? (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 2E-12
Odds Ratio 0.1619 [0.11-0.21] unit increase


[PMID 26520901] Impact of carotid atherosclerosis loci on cardiovascular events