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rs17774966

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs17774966(C;T)
Make rs17774966(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position25551359
is asnp
is mentioned by
dbSNPrs17774966
ebirs17774966
HLIrs17774966
Exacrs17774966
Varsomers17774966
Maprs17774966
PheGenIrs17774966
hapmaprs17774966
1000 genomesrs17774966
hgdprs17774966
ensemblrs17774966
gopubmedrs17774966
geneviewrs17774966
scholarrs17774966
googlers17774966
pharmgkbrs17774966
gwascentralrs17774966
openSNPrs17774966
23andMers17774966
23andMe allrs17774966
SNP Nexus

SNPshotrs17774966
SNPdbers17774966
MSV3drs17774966
GWAS Ctlgrs17774966
GMAF0.09229
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21116278]
Trait
Title Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease
Risk Allele
P-val 0.000008
Odds Ratio 0.1530 [NR] unit increase (interaction)