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rs2969775

From SNPedia

Orientationminus
Stabilizedminus
Make rs2969775(A;A)
Make rs2969775(A;C)
Make rs2969775(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47658337
is asnp
is mentioned by
dbSNPrs2969775
ebirs2969775
HLIrs2969775
Exacrs2969775
Varsomers2969775
Maprs2969775
PheGenIrs2969775
hapmaprs2969775
1000 genomesrs2969775
hgdprs2969775
ensemblrs2969775
gopubmedrs2969775
geneviewrs2969775
scholarrs2969775
googlers2969775
pharmgkbrs2969775
gwascentralrs2969775
openSNPrs2969775
23andMers2969775
23andMe allrs2969775
SNP Nexus

SNPshotrs2969775
SNPdbers2969775
MSV3drs2969775
GWAS Ctlgrs2969775
GMAF0.2879
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22005930OA-icon.png]
Trait
Title Genome-wide association study of Alzheimer's disease with psychotic symptoms.
Risk Allele
P-val 0.000002
Odds Ratio 1.4700 None