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rs17189298

From SNPedia

Orientationplus
Stabilizedplus
Make rs17189298(A;A)
Make rs17189298(A;G)
Make rs17189298(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position119087741
is asnp
is mentioned by
dbSNPrs17189298
ebirs17189298
HLIrs17189298
Exacrs17189298
Varsomers17189298
Maprs17189298
PheGenIrs17189298
hapmaprs17189298
1000 genomesrs17189298
hgdprs17189298
ensemblrs17189298
gopubmedrs17189298
geneviewrs17189298
scholarrs17189298
googlers17189298
pharmgkbrs17189298
gwascentralrs17189298
openSNPrs17189298
23andMers17189298
23andMe allrs17189298
SNP Nexus

SNPshotrs17189298
SNPdbers17189298
MSV3drs17189298
GWAS Ctlgrs17189298
GMAF0.3489
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20932310OA-icon.png]
Trait
Title Genome-wide association reveals genetic effects on human Abeta42 and tau protein levels in cerebrospinal fluids: a case control study
Risk Allele A
P-val 3E-7
Odds Ratio None None