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rs6602175

From SNPedia

Orientationplus
Stabilizedplus
Make rs6602175(G;G)
Make rs6602175(G;T)
Make rs6602175(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position17100527
GeneCUBN
is asnp
is mentioned by
dbSNPrs6602175
ebirs6602175
HLIrs6602175
Exacrs6602175
Varsomers6602175
Maprs6602175
PheGenIrs6602175
hapmaprs6602175
1000 genomesrs6602175
hgdprs6602175
ensemblrs6602175
gopubmedrs6602175
geneviewrs6602175
scholarrs6602175
googlers6602175
pharmgkbrs6602175
gwascentralrs6602175
openSNPrs6602175
23andMers6602175
23andMe allrs6602175
SNP Nexus

SNPshotrs6602175
SNPdbers6602175
MSV3drs6602175
GWAS Ctlgrs6602175
GMAF0.4197
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 0.000003
Odds Ratio 0.0075 [NR] unit decrease (main effect)