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rs732528

From SNPedia

Orientationminus
Stabilizedminus
Make rs732528(A;A)
Make rs732528(A;G)
Make rs732528(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position50851864
is asnp
is mentioned by
dbSNPrs732528
dbSNP (classic)rs732528
ClinGenrs732528
ebirs732528
HLIrs732528
Exacrs732528
Gnomadrs732528
Varsomers732528
LitVarrs732528
Maprs732528
PheGenIrs732528
Biobankrs732528
1000 genomesrs732528
hgdprs732528
ensemblrs732528
geneviewrs732528
scholarrs732528
googlers732528
pharmgkbrs732528
gwascentralrs732528
openSNPrs732528
23andMers732528
SNPshotrs732528
SNPdbers732528
MSV3drs732528
GWAS Ctlgrs732528
GMAF0.1837
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 21116278OA-icon.png]
Trait
Title Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease
Risk Allele
P-val 0.000007
Odds Ratio 0.1106 [NR] unit decrease (main effect)