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rs16970672

From SNPedia

Orientationplus
Stabilizedplus
Make rs16970672(A;A)
Make rs16970672(A;G)
Make rs16970672(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position77948568
is asnp
is mentioned by
dbSNPrs16970672
ebirs16970672
HLIrs16970672
Exacrs16970672
Varsomers16970672
Maprs16970672
PheGenIrs16970672
hapmaprs16970672
1000 genomesrs16970672
hgdprs16970672
ensemblrs16970672
gopubmedrs16970672
geneviewrs16970672
scholarrs16970672
googlers16970672
pharmgkbrs16970672
gwascentralrs16970672
openSNPrs16970672
23andMers16970672
23andMe allrs16970672
SNP Nexus

SNPshotrs16970672
SNPdbers16970672
MSV3drs16970672
GWAS Ctlgrs16970672
GMAF0.3246
Max Magnitude
? (A;A) (A;G) (G;G) 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 1.2900 None