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rs10512049

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10512049(C;T)
Make rs10512049(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position75661759
is asnp
is mentioned by
dbSNPrs10512049
ebirs10512049
HLIrs10512049
Exacrs10512049
Varsomers10512049
Maprs10512049
PheGenIrs10512049
hapmaprs10512049
1000 genomesrs10512049
hgdprs10512049
ensemblrs10512049
gopubmedrs10512049
geneviewrs10512049
scholarrs10512049
googlers10512049
pharmgkbrs10512049
gwascentralrs10512049
openSNPrs10512049
23andMers10512049
23andMe allrs10512049
SNP Nexus

SNPshotrs10512049
SNPdbers10512049
MSV3drs10512049
GWAS Ctlgrs10512049
GMAF0.04959
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 0.000003
Odds Ratio 0.0072 [NR] unit decrease (interaction)