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rs2852894

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2852894(C;T)
Make rs2852894(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position102284743
is asnp
is mentioned by
dbSNPrs2852894
dbSNP (classic)rs2852894
ClinGenrs2852894
ebirs2852894
HLIrs2852894
Exacrs2852894
Gnomadrs2852894
Varsomers2852894
LitVarrs2852894
Maprs2852894
PheGenIrs2852894
Biobankrs2852894
1000 genomesrs2852894
hgdprs2852894
ensemblrs2852894
geneviewrs2852894
scholarrs2852894
googlers2852894
pharmgkbrs2852894
gwascentralrs2852894
openSNPrs2852894
23andMers2852894
SNPshotrs2852894
SNPdbers2852894
MSV3drs2852894
GWAS Ctlgrs2852894
GMAF0.04821
Max Magnitude0
? (C;C) (C;T) (T;T) 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 0.000001
Odds Ratio 0.0163 [NR] unit decrease (interaction)