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rs11129640

From SNPedia

Orientationplus
Stabilizedplus
Make rs11129640(G;G)
Make rs11129640(G;T)
Make rs11129640(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position35101019
GeneLOC101928135
is asnp
is mentioned by
dbSNPrs11129640
ebirs11129640
HLIrs11129640
Exacrs11129640
Varsomers11129640
Maprs11129640
PheGenIrs11129640
hapmaprs11129640
1000 genomesrs11129640
hgdprs11129640
ensemblrs11129640
gopubmedrs11129640
geneviewrs11129640
scholarrs11129640
googlers11129640
pharmgkbrs11129640
gwascentralrs11129640
openSNPrs11129640
23andMers11129640
23andMe allrs11129640
SNP Nexus

SNPshotrs11129640
SNPdbers11129640
MSV3drs11129640
GWAS Ctlgrs11129640
GMAF0.2383
Max Magnitude
? (G;G) (G;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 6E-8
Odds Ratio 0.1232 [NR] unit decrease (main effect)